Skip to main content
Top
Published in: Journal of Inherited Metabolic Disease 6/2017

Open Access 01-11-2017 | Review

Epidemiology, diagnosis, and treatment of cerebrotendinous xanthomatosis (CTX)

Authors: Gerald Salen, Robert D. Steiner

Published in: Journal of Inherited Metabolic Disease | Issue 6/2017

Login to get access

Abstract

Cerebrotendinous xanthomatosis (CTX) is a rare autosomal recessive disorder of bile acid synthesis caused by mutations in the cytochrome P450 CYP27A1 gene that result in production of a defective sterol 27-hydroxylase enzyme. CTX is associated with abnormally high levels of cholestanol in the blood and accumulation of cholestanol and cholesterol in the brain, tendon xanthomas, and bile. Hallmark clinical manifestations of CTX include chronic diarrhea, bilateral cataracts, tendon xanthomas, and neurologic dysfunction. Although CTX is a rare disorder, it is thought to be underdiagnosed, as presenting signs and symptoms may be nonspecific with significant overlap with other more common conditions. There is marked variability in signs and symptoms, severity, and age of onset between patients. The disease course is progressive and potentially debilitating or fatal, particularly with respect to neurologic presentations that can include intellectual disability, autism, behavioral and psychiatric problems, and dementia, among others. Treatment with chenodeoxycholic acid (CDCA; chenodiol) is the current standard of care. CDCA can help restore normal sterol, bile acid, bile alcohol, and cholestanol levels. CDCA also appears to be generally effective in preventing adverse clinical manifestations of the disease from occurring or progressing if administered early enough. Improved screening and awareness of the condition may help facilitate early diagnosis and treatment.
Literature
go back to reference Appadurai V, DeBarber A, Chiang PW et al (2015) Apparent underdiagnosis of Cerebrotendinous Xanthomatosis revealed by analysis of ~60,000 human exomes. Mol Genet Metab 116:298–304CrossRefPubMedPubMedCentral Appadurai V, DeBarber A, Chiang PW et al (2015) Apparent underdiagnosis of Cerebrotendinous Xanthomatosis revealed by analysis of ~60,000 human exomes. Mol Genet Metab 116:298–304CrossRefPubMedPubMedCentral
go back to reference Ballantyne CM, Vega GL, East C, Richards G, Grundy SM (1987) Low-density lipoprotein metabolism in cerebrotendinous xanthomatosis. Metabolism 36:270–276CrossRefPubMed Ballantyne CM, Vega GL, East C, Richards G, Grundy SM (1987) Low-density lipoprotein metabolism in cerebrotendinous xanthomatosis. Metabolism 36:270–276CrossRefPubMed
go back to reference Batta AK, Salen G, Shefer S, Tint GS, Batta M (1987) Increased plasma bile alcohol glucuronides in patients with cerebrotendinous xanthomatosis: effect of chenodeoxycholic acid. J Lipid Res 28:1006–1012PubMed Batta AK, Salen G, Shefer S, Tint GS, Batta M (1987) Increased plasma bile alcohol glucuronides in patients with cerebrotendinous xanthomatosis: effect of chenodeoxycholic acid. J Lipid Res 28:1006–1012PubMed
go back to reference Batta AK, Salen G, Tint GS (2004) Hydrophilic 7 beta-hydroxy bile acids, lovastatin, and cholestyramine are ineffective in the treatment of cerebrotendinous xanthomatosis. Metabolism 53:556–562CrossRefPubMed Batta AK, Salen G, Tint GS (2004) Hydrophilic 7 beta-hydroxy bile acids, lovastatin, and cholestyramine are ineffective in the treatment of cerebrotendinous xanthomatosis. Metabolism 53:556–562CrossRefPubMed
go back to reference Bavner A, Shafaati M, Hansson M et al (2010) On the mechanism of accumulation of cholestanol in the brain of mice with a disruption of sterol 27-hydroxylase. J Lipid Res 51:2722–2730CrossRefPubMedPubMedCentral Bavner A, Shafaati M, Hansson M et al (2010) On the mechanism of accumulation of cholestanol in the brain of mice with a disruption of sterol 27-hydroxylase. J Lipid Res 51:2722–2730CrossRefPubMedPubMedCentral
go back to reference Beppu T, Seyama Y, Kasama T, Serizawa S, Yamakawa T (1982) Serum bile acid profiles in cerebrotendinous xanthomatosis. Clin Chim Acta 118:167–175CrossRefPubMed Beppu T, Seyama Y, Kasama T, Serizawa S, Yamakawa T (1982) Serum bile acid profiles in cerebrotendinous xanthomatosis. Clin Chim Acta 118:167–175CrossRefPubMed
go back to reference Berginer VM, Abeliovich D (1981) Genetics of cerebrotendinous xanthomatosis (CTX): an autosomal recessive trait with high gene frequency in Sephardim of Moroccan origin. Am J Med Genet 10:151–157CrossRefPubMed Berginer VM, Abeliovich D (1981) Genetics of cerebrotendinous xanthomatosis (CTX): an autosomal recessive trait with high gene frequency in Sephardim of Moroccan origin. Am J Med Genet 10:151–157CrossRefPubMed
go back to reference Berginer VM, Radwan H, Korczyn AD, Kott E, Salen G, Shefer S (1982) EEG in cerebrotendinous xanthomatosis (CTX). Clin Electroencephalogr 13:89–96CrossRefPubMed Berginer VM, Radwan H, Korczyn AD, Kott E, Salen G, Shefer S (1982) EEG in cerebrotendinous xanthomatosis (CTX). Clin Electroencephalogr 13:89–96CrossRefPubMed
go back to reference Berginer VM, Salen G, Shefer S (1984) Long-term treatment of cerebrotendinous xanthomatosis with chenodeoxycholic acid. N Engl J Med 311:1649–1652CrossRefPubMed Berginer VM, Salen G, Shefer S (1984) Long-term treatment of cerebrotendinous xanthomatosis with chenodeoxycholic acid. N Engl J Med 311:1649–1652CrossRefPubMed
go back to reference Berginer VM, Carmi R, Salen G (1988) Pregnancy in women with cerebrotendinous xanthomatosis (CTX): high risk condition for fetus and newborn infant? Am J Med Genet 31:11–16CrossRefPubMed Berginer VM, Carmi R, Salen G (1988) Pregnancy in women with cerebrotendinous xanthomatosis (CTX): high risk condition for fetus and newborn infant? Am J Med Genet 31:11–16CrossRefPubMed
go back to reference Berginer VM, Shany S, Alkalay D et al (1993) Osteoporosis and increased bone fractures in cerebrotendinous xanthomatosis. Metabolism 42:69–74CrossRefPubMed Berginer VM, Shany S, Alkalay D et al (1993) Osteoporosis and increased bone fractures in cerebrotendinous xanthomatosis. Metabolism 42:69–74CrossRefPubMed
go back to reference Berginer VM, Berginer J, Korczyn AD, Tadmor R (1994) Magnetic resonance imaging in cerebrotendinous xanthomatosis: a prospective clinical and neuroradiological study. J Neurol Sci 122:102–108CrossRefPubMed Berginer VM, Berginer J, Korczyn AD, Tadmor R (1994) Magnetic resonance imaging in cerebrotendinous xanthomatosis: a prospective clinical and neuroradiological study. J Neurol Sci 122:102–108CrossRefPubMed
go back to reference Berginer VM, Gross B, Morad K et al (2009) Chronic diarrhea and juvenile cataracts: think cerebrotendinous xanthomatosis and treat. Pediatrics 123:143–147CrossRefPubMed Berginer VM, Gross B, Morad K et al (2009) Chronic diarrhea and juvenile cataracts: think cerebrotendinous xanthomatosis and treat. Pediatrics 123:143–147CrossRefPubMed
go back to reference Berginer VM, Salen G, Patel SB (2015) Cerebrotendinous xanthomatosis. In: Rosenberg RN, Pascual JM (eds) Rosenberg's molecular and genetic basis of neurological and psychiatric disease. Elsevier, London, pp 589–598CrossRef Berginer VM, Salen G, Patel SB (2015) Cerebrotendinous xanthomatosis. In: Rosenberg RN, Pascual JM (eds) Rosenberg's molecular and genetic basis of neurological and psychiatric disease. Elsevier, London, pp 589–598CrossRef
go back to reference Bhattacharyya AK, Lin DS, Connor WE (2007) Cholestanol metabolism in patients with cerebrotendinous xanthomatosis: absorption, turnover, and tissue deposition. J Lipid Res 48:185–192CrossRefPubMed Bhattacharyya AK, Lin DS, Connor WE (2007) Cholestanol metabolism in patients with cerebrotendinous xanthomatosis: absorption, turnover, and tissue deposition. J Lipid Res 48:185–192CrossRefPubMed
go back to reference Björkhem I, Hansson M (2010) Cerebrotendinous xanthomatosis: an inborn error in bile acid synthesis with defined mutations but still a challenge. Biochem Biophys Res Commun 396:46–49CrossRefPubMed Björkhem I, Hansson M (2010) Cerebrotendinous xanthomatosis: an inborn error in bile acid synthesis with defined mutations but still a challenge. Biochem Biophys Res Commun 396:46–49CrossRefPubMed
go back to reference Björkhem I, Skrede S, Buchmann MS, East C, Grundy S (1987) Accumulation of 7 alpha-hydroxy-4-cholesten-3-one and cholesta-4,6-dien-3-one in patients with cerebrotendinous xanthomatosis: effect of treatment with chenodeoxycholic acid. Hepatology 7:266–271CrossRefPubMed Björkhem I, Skrede S, Buchmann MS, East C, Grundy S (1987) Accumulation of 7 alpha-hydroxy-4-cholesten-3-one and cholesta-4,6-dien-3-one in patients with cerebrotendinous xanthomatosis: effect of treatment with chenodeoxycholic acid. Hepatology 7:266–271CrossRefPubMed
go back to reference Björkhem I, Diczfalusy U, Lovgren-Sandblom A et al (2014) On the formation of 7-ketocholesterol from 7-dehydrocholesterol in patients with CTX and SLO. J Lipid Res 55:1165–1172CrossRefPubMedPubMedCentral Björkhem I, Diczfalusy U, Lovgren-Sandblom A et al (2014) On the formation of 7-ketocholesterol from 7-dehydrocholesterol in patients with CTX and SLO. J Lipid Res 55:1165–1172CrossRefPubMedPubMedCentral
go back to reference Bleyle L, Huidekoper HH, Vaz FM, Singh R, Steiner RD, DeBarber AE (2016) Update on newborn dried bloodspot testing for cerebrotendinous xanthomatosis: an available high-throughput liquid-chromatography tandem mass spectrometry method. Mol Genet Metab Rep 7:11–15CrossRefPubMedPubMedCentral Bleyle L, Huidekoper HH, Vaz FM, Singh R, Steiner RD, DeBarber AE (2016) Update on newborn dried bloodspot testing for cerebrotendinous xanthomatosis: an available high-throughput liquid-chromatography tandem mass spectrometry method. Mol Genet Metab Rep 7:11–15CrossRefPubMedPubMedCentral
go back to reference Brienza M, Fiermonte G, Cambieri C, Mignarri A, Dotti MT, Fiorelli M (2015) Enlarging brain xanthomas in a patient with cerebrotendinous xanthomatosis. J Inherit Metab Dis 38:981–982CrossRefPubMed Brienza M, Fiermonte G, Cambieri C, Mignarri A, Dotti MT, Fiorelli M (2015) Enlarging brain xanthomas in a patient with cerebrotendinous xanthomatosis. J Inherit Metab Dis 38:981–982CrossRefPubMed
go back to reference Cali JJ, Hsieh CL, Francke U, Russell DW (1991) Mutations in the bile acid biosynthetic enzyme sterol 27-hydroxylase underlie cerebrotendinous xanthomatosis. J Biol Chem 266:7779–7783PubMedPubMedCentral Cali JJ, Hsieh CL, Francke U, Russell DW (1991) Mutations in the bile acid biosynthetic enzyme sterol 27-hydroxylase underlie cerebrotendinous xanthomatosis. J Biol Chem 266:7779–7783PubMedPubMedCentral
go back to reference Chenodal™ 250 mg (chenodiol tablets) [prescribing information] (2009) Manchester Pharmaceuticals, Inc, Fort Collins Chenodal™ 250 mg (chenodiol tablets) [prescribing information] (2009) Manchester Pharmaceuticals, Inc, Fort Collins
go back to reference Clayton PT, Verrips A, Sistermans E, Mann A, Mieli-Vergani G, Wevers R (2002) Mutations in the sterol 27-hydroxylase gene (CYP27A) cause hepatitis of infancy as well as cerebrotendinous xanthomatosis. J Inherit Metab Dis 25:501–513CrossRefPubMed Clayton PT, Verrips A, Sistermans E, Mann A, Mieli-Vergani G, Wevers R (2002) Mutations in the sterol 27-hydroxylase gene (CYP27A) cause hepatitis of infancy as well as cerebrotendinous xanthomatosis. J Inherit Metab Dis 25:501–513CrossRefPubMed
go back to reference Cruysberg JR, Wevers RA, Tolboom JJ (1991) Juvenile cataract associated with chronic diarrhea in pediatric cerebrotendinous xanthomatosis. Am J Ophthalmol 112:606–607CrossRefPubMed Cruysberg JR, Wevers RA, Tolboom JJ (1991) Juvenile cataract associated with chronic diarrhea in pediatric cerebrotendinous xanthomatosis. Am J Ophthalmol 112:606–607CrossRefPubMed
go back to reference Cruysberg JR, Wevers RA, van Engelen BG, Pinckers A, van Spreeken A, Tolboom JJ (1995) Ocular and systemic manifestations of cerebrotendinous xanthomatosis. Am J Ophthalmol 120:597–604CrossRefPubMed Cruysberg JR, Wevers RA, van Engelen BG, Pinckers A, van Spreeken A, Tolboom JJ (1995) Ocular and systemic manifestations of cerebrotendinous xanthomatosis. Am J Ophthalmol 120:597–604CrossRefPubMed
go back to reference De Stefano N, Dotti MT, Mortilla M, Federico A (2001) Magnetic resonance imaging and spectroscopic changes in brains of patients with cerebrotendinous xanthomatosis. Brain 124:121–131CrossRefPubMed De Stefano N, Dotti MT, Mortilla M, Federico A (2001) Magnetic resonance imaging and spectroscopic changes in brains of patients with cerebrotendinous xanthomatosis. Brain 124:121–131CrossRefPubMed
go back to reference DeBarber AE, Connor WE, Pappu AS, Merkens LS, Steiner RD (2010) ESI-MS/MS quantification of 7alpha-hydroxy-4-cholesten-3-one facilitates rapid, convenient diagnostic testing for cerebrotendinous xanthomatosis. Clin Chim Acta 411:43–48CrossRefPubMed DeBarber AE, Connor WE, Pappu AS, Merkens LS, Steiner RD (2010) ESI-MS/MS quantification of 7alpha-hydroxy-4-cholesten-3-one facilitates rapid, convenient diagnostic testing for cerebrotendinous xanthomatosis. Clin Chim Acta 411:43–48CrossRefPubMed
go back to reference DeBarber AE, Sandlers Y, Pappu AS et al (2011) Profiling sterols in cerebrotendinous xanthomatosis: utility of Girard derivatization and high resolution exact mass LC-ESI-MS(n) analysis. J Chromatogr B Anal Technol Biomed Life Sci 879:1384–1392CrossRef DeBarber AE, Sandlers Y, Pappu AS et al (2011) Profiling sterols in cerebrotendinous xanthomatosis: utility of Girard derivatization and high resolution exact mass LC-ESI-MS(n) analysis. J Chromatogr B Anal Technol Biomed Life Sci 879:1384–1392CrossRef
go back to reference DeBarber AE, Luo J, Star-Weinstock M et al (2014b) A blood test for cerebrotendinous xanthomatosis with potential for disease detection in newborns. J Lipid Res 55:146–154CrossRefPubMedPubMedCentral DeBarber AE, Luo J, Star-Weinstock M et al (2014b) A blood test for cerebrotendinous xanthomatosis with potential for disease detection in newborns. J Lipid Res 55:146–154CrossRefPubMedPubMedCentral
go back to reference Degos B, Nadjar Y, Amador MM et al (2016) Natural history of cerebrotendinous xanthomatosis: a paediatric disease diagnosed in adulthood. Orphanet J Rare Dis 11:41CrossRefPubMedPubMedCentral Degos B, Nadjar Y, Amador MM et al (2016) Natural history of cerebrotendinous xanthomatosis: a paediatric disease diagnosed in adulthood. Orphanet J Rare Dis 11:41CrossRefPubMedPubMedCentral
go back to reference Dotti MT, Rufa A, Federico A (2001) Cerebrotendinous xanthomatosis: heterogeneity of clinical phenotype with evidence of previously undescribed ophthalmological findings. J Inherit Metab Dis 24:696–706CrossRefPubMed Dotti MT, Rufa A, Federico A (2001) Cerebrotendinous xanthomatosis: heterogeneity of clinical phenotype with evidence of previously undescribed ophthalmological findings. J Inherit Metab Dis 24:696–706CrossRefPubMed
go back to reference Dotti MT, Lutjohann D, von Bergmann K, Federico A (2004) Normalisation of serum cholestanol concentration in a patient with cerebrotendinous xanthomatosis by combined treatment with chenodeoxycholic acid, simvastatin and LDL apheresis. Neurol Sci 25:185–191CrossRefPubMed Dotti MT, Lutjohann D, von Bergmann K, Federico A (2004) Normalisation of serum cholestanol concentration in a patient with cerebrotendinous xanthomatosis by combined treatment with chenodeoxycholic acid, simvastatin and LDL apheresis. Neurol Sci 25:185–191CrossRefPubMed
go back to reference Einarsson C, Hillebrant CG, Axelson M (2001) Effects of treatment with deoxycholic acid and chenodeoxycholic acid on the hepatic synthesis of cholesterol and bile acids in healthy subjects. Hepatology 33:1189–1193CrossRefPubMed Einarsson C, Hillebrant CG, Axelson M (2001) Effects of treatment with deoxycholic acid and chenodeoxycholic acid on the hepatic synthesis of cholesterol and bile acids in healthy subjects. Hepatology 33:1189–1193CrossRefPubMed
go back to reference Ellis E, Axelson M, Abrahamsson A et al (2003) Feedback regulation of bile acid synthesis in primary human hepatocytes: evidence that CDCA is the strongest inhibitor. Hepatology 38:930–938CrossRefPubMed Ellis E, Axelson M, Abrahamsson A et al (2003) Feedback regulation of bile acid synthesis in primary human hepatocytes: evidence that CDCA is the strongest inhibitor. Hepatology 38:930–938CrossRefPubMed
go back to reference Embirucu EK, Otaduy MC, Taneja AK, Leite CC, Kok F, Lucato LT (2010) MR spectroscopy detects lipid peaks in cerebrotendinous xanthomatosis. AJNR Am J Neuroradiol 31:1347–1349CrossRefPubMed Embirucu EK, Otaduy MC, Taneja AK, Leite CC, Kok F, Lucato LT (2010) MR spectroscopy detects lipid peaks in cerebrotendinous xanthomatosis. AJNR Am J Neuroradiol 31:1347–1349CrossRefPubMed
go back to reference Falik-Zaccai TC, Kfir N, Frenkel P et al (2008) Population screening in a Druze community: the challenge and the reward. Genet Med 10:903–909CrossRefPubMed Falik-Zaccai TC, Kfir N, Frenkel P et al (2008) Population screening in a Druze community: the challenge and the reward. Genet Med 10:903–909CrossRefPubMed
go back to reference Federico A, Dotti MT, Lore F, Nuti R (1993) Cerebrotendinous xanthomatosis: pathophysiological study on bone metabolism. J Neurol Sci 115:67–70CrossRefPubMed Federico A, Dotti MT, Lore F, Nuti R (1993) Cerebrotendinous xanthomatosis: pathophysiological study on bone metabolism. J Neurol Sci 115:67–70CrossRefPubMed
go back to reference Fujiyama J, Kuriyama M, Arima S et al (1991) Atherogenic risk factors in cerebrotendinous xanthomatosis. Clin Chim Acta 200:1–11CrossRefPubMed Fujiyama J, Kuriyama M, Arima S et al (1991) Atherogenic risk factors in cerebrotendinous xanthomatosis. Clin Chim Acta 200:1–11CrossRefPubMed
go back to reference Ginanneschi F, Mignarri A, Mondelli M et al (2013) Polyneuropathy in cerebrotendinous xanthomatosis and response to treatment with chenodeoxycholic acid. J Neurol 260:268–274CrossRefPubMed Ginanneschi F, Mignarri A, Mondelli M et al (2013) Polyneuropathy in cerebrotendinous xanthomatosis and response to treatment with chenodeoxycholic acid. J Neurol 260:268–274CrossRefPubMed
go back to reference Giraldo-Chica M, Acosta-Baena N, Urbano L, Velilla L, Lopera F, Pineda N (2015) Novel cerebrotendinous xanthomatosis mutation causes familial early dementia in Colombia. Biomedica 35:563–571CrossRefPubMed Giraldo-Chica M, Acosta-Baena N, Urbano L, Velilla L, Lopera F, Pineda N (2015) Novel cerebrotendinous xanthomatosis mutation causes familial early dementia in Colombia. Biomedica 35:563–571CrossRefPubMed
go back to reference Guerrera S, Stromillo ML, Mignarri A et al (2010) Clinical relevance of brain volume changes in patients with cerebrotendinous xanthomatosis. J Neurol Neurosurg Psychiatry 81:1189–1193CrossRefPubMed Guerrera S, Stromillo ML, Mignarri A et al (2010) Clinical relevance of brain volume changes in patients with cerebrotendinous xanthomatosis. J Neurol Neurosurg Psychiatry 81:1189–1193CrossRefPubMed
go back to reference Hoshita T, Yasuhara M, Une M et al (1980) Occurrence of bile alcohol glucuronides in bile of patients with cerebrotendinous xanthomatosis. J Lipid Res 21:1015–1021PubMed Hoshita T, Yasuhara M, Une M et al (1980) Occurrence of bile alcohol glucuronides in bile of patients with cerebrotendinous xanthomatosis. J Lipid Res 21:1015–1021PubMed
go back to reference Huidekoper HH, Vaz FM, Verrips A, Bosch AM (2016) Hepatotoxicity due to chenodeoxycholic acid supplementation in an infant with cerebrotendinous xanthomatosis: implications for treatment. Eur J Pediatr 175:143–146CrossRefPubMed Huidekoper HH, Vaz FM, Verrips A, Bosch AM (2016) Hepatotoxicity due to chenodeoxycholic acid supplementation in an infant with cerebrotendinous xanthomatosis: implications for treatment. Eur J Pediatr 175:143–146CrossRefPubMed
go back to reference Kawabata M, Kuriyama M, Mori S, Sakashita I, Osame M (1998) Pulmonary manifestations in cerebrotendinous xanthomatosis. Intern Med 37:922–926CrossRefPubMed Kawabata M, Kuriyama M, Mori S, Sakashita I, Osame M (1998) Pulmonary manifestations in cerebrotendinous xanthomatosis. Intern Med 37:922–926CrossRefPubMed
go back to reference Kinoshita M, Kawamura M, Fujita M et al (2004) Enhanced susceptibility of LDL to oxidative modification in a CTX patient:- role of chenodeoxycholic acid in xanthoma formation. J Atheroscler Thromb 11:167–172CrossRefPubMed Kinoshita M, Kawamura M, Fujita M et al (2004) Enhanced susceptibility of LDL to oxidative modification in a CTX patient:- role of chenodeoxycholic acid in xanthoma formation. J Atheroscler Thromb 11:167–172CrossRefPubMed
go back to reference Koopman BJ, Wolthers BG, van der Molen JC, Waterreus RJ (1985) Bile acid therapies applied to patients suffering from cerebrotendinous xanthomatosis. Clin Chim Acta 152:115–122CrossRefPubMed Koopman BJ, Wolthers BG, van der Molen JC, Waterreus RJ (1985) Bile acid therapies applied to patients suffering from cerebrotendinous xanthomatosis. Clin Chim Acta 152:115–122CrossRefPubMed
go back to reference Kuriyama M, Fujiyama J, Kasama T, Osame M (1991a) High levels of plant sterols and cholesterol precursors in cerebrotendinous xanthomatosis. J Lipid Res 32:223–229PubMed Kuriyama M, Fujiyama J, Kasama T, Osame M (1991a) High levels of plant sterols and cholesterol precursors in cerebrotendinous xanthomatosis. J Lipid Res 32:223–229PubMed
go back to reference Kuriyama M, Fujiyama J, Yoshidome H et al (1991b) Cerebrotendinous xanthomatosis: clinical and biochemical evaluation of eight patients and review of the literature. J Neurol Sci 102:225–232CrossRefPubMed Kuriyama M, Fujiyama J, Yoshidome H et al (1991b) Cerebrotendinous xanthomatosis: clinical and biochemical evaluation of eight patients and review of the literature. J Neurol Sci 102:225–232CrossRefPubMed
go back to reference Kuriyama M, Tokimura Y, Fujiyama J, Utatsu Y, Osame M (1994) Treatment of cerebrotendinous xanthomatosis: effects of chenodeoxycholic acid, pravastatin, and combined use. J Neurol Sci 125:22–28CrossRefPubMed Kuriyama M, Tokimura Y, Fujiyama J, Utatsu Y, Osame M (1994) Treatment of cerebrotendinous xanthomatosis: effects of chenodeoxycholic acid, pravastatin, and combined use. J Neurol Sci 125:22–28CrossRefPubMed
go back to reference Larson A, Weisfeld-Adams JD, Benke TA, Bonnen PE (2017) Cerebrotendinous xanthomatosis presenting with infantile spasms and intellectual disability. JIMD Rep 35:1–5PubMed Larson A, Weisfeld-Adams JD, Benke TA, Bonnen PE (2017) Cerebrotendinous xanthomatosis presenting with infantile spasms and intellectual disability. JIMD Rep 35:1–5PubMed
go back to reference Leitersdorf E, Reshef A, Meiner V et al (1993) Frameshift and splice-junction mutations in the sterol 27-hydroxylase gene cause cerebrotendinous xanthomatosis in Jews or Moroccan origin. J Clin Invest 91:2488–2496CrossRefPubMedPubMedCentral Leitersdorf E, Reshef A, Meiner V et al (1993) Frameshift and splice-junction mutations in the sterol 27-hydroxylase gene cause cerebrotendinous xanthomatosis in Jews or Moroccan origin. J Clin Invest 91:2488–2496CrossRefPubMedPubMedCentral
go back to reference Lorbek G, Lewinska M, Rozman D (2012) Cytochrome P450s in the synthesis of cholesterol and bile acids--from mouse models to human diseases. FEBS J 279:1516–1533CrossRefPubMed Lorbek G, Lewinska M, Rozman D (2012) Cytochrome P450s in the synthesis of cholesterol and bile acids--from mouse models to human diseases. FEBS J 279:1516–1533CrossRefPubMed
go back to reference Lorincz MT, Rainier S, Thomas D, Fink JK (2005) Cerebrotendinous xanthomatosis: possible higher prevalence than previously recognized. Arch Neurol 62:1459–1463CrossRefPubMed Lorincz MT, Rainier S, Thomas D, Fink JK (2005) Cerebrotendinous xanthomatosis: possible higher prevalence than previously recognized. Arch Neurol 62:1459–1463CrossRefPubMed
go back to reference Ly H, Bertorini TE, Shah N (2014) An adult male with progressive spastic paraparesis and gait instability. J Clin Neuromuscul Dis 16:98–103CrossRefPubMed Ly H, Bertorini TE, Shah N (2014) An adult male with progressive spastic paraparesis and gait instability. J Clin Neuromuscul Dis 16:98–103CrossRefPubMed
go back to reference Martini G, Mignarri A, Ruvio M et al (2013) Long-term bone density evaluation in cerebrotendinous xanthomatosis: evidence of improvement after chenodeoxycholic acid treatment. Calcif Tissue Int 92:282–286CrossRefPubMed Martini G, Mignarri A, Ruvio M et al (2013) Long-term bone density evaluation in cerebrotendinous xanthomatosis: evidence of improvement after chenodeoxycholic acid treatment. Calcif Tissue Int 92:282–286CrossRefPubMed
go back to reference Mignarri A, Gallus GN, Dotti MT, Federico A (2014) A suspicion index for early diagnosis and treatment of cerebrotendinous xanthomatosis. J Inherit Metab Dis 37:421–429CrossRefPubMed Mignarri A, Gallus GN, Dotti MT, Federico A (2014) A suspicion index for early diagnosis and treatment of cerebrotendinous xanthomatosis. J Inherit Metab Dis 37:421–429CrossRefPubMed
go back to reference Mignarri A, Magni A, Del Puppo M et al (2016) Evaluation of cholesterol metabolism in cerebrotendinous xanthomatosis. J Inherit Metab Dis 39:75–83CrossRefPubMed Mignarri A, Magni A, Del Puppo M et al (2016) Evaluation of cholesterol metabolism in cerebrotendinous xanthomatosis. J Inherit Metab Dis 39:75–83CrossRefPubMed
go back to reference Mimura Y, Kuriyama M, Tokimura Y et al (1993) Treatment of cerebrotendinous xanthomatosis with low-density lipoprotein (LDL)-apheresis. J Neurol Sci 114:227–230CrossRefPubMed Mimura Y, Kuriyama M, Tokimura Y et al (1993) Treatment of cerebrotendinous xanthomatosis with low-density lipoprotein (LDL)-apheresis. J Neurol Sci 114:227–230CrossRefPubMed
go back to reference Moghadasian MH (2004) Cerebrotendinous xanthomatosis: clinical course, genotypes and metabolic backgrounds. Clin Invest Med 27:42–50PubMed Moghadasian MH (2004) Cerebrotendinous xanthomatosis: clinical course, genotypes and metabolic backgrounds. Clin Invest Med 27:42–50PubMed
go back to reference Moghadasian MH, Salen G, Frohlich JJ, Scudamore CH (2002) Cerebrotendinous xanthomatosis: a rare disease with diverse manifestations. Arch Neurol 59:527–529CrossRefPubMed Moghadasian MH, Salen G, Frohlich JJ, Scudamore CH (2002) Cerebrotendinous xanthomatosis: a rare disease with diverse manifestations. Arch Neurol 59:527–529CrossRefPubMed
go back to reference Mondelli M, Rossi A, Scarpini C, Dotti MT, Federico A (1992) Evoked potentials in cerebrotendinous xanthomatosis and effect induced by chenodeoxycholic acid. Arch Neurol 49:469–475CrossRefPubMed Mondelli M, Rossi A, Scarpini C, Dotti MT, Federico A (1992) Evoked potentials in cerebrotendinous xanthomatosis and effect induced by chenodeoxycholic acid. Arch Neurol 49:469–475CrossRefPubMed
go back to reference Mondelli M, Sicurelli F, Scarpini C, Dotti MT, Federico A (2001) Cerebrotendinous xanthomatosis: 11-year treatment with chenodeoxycholic acid in five patients. An electrophysiological study. J Neurol Sci 190:29–33CrossRefPubMed Mondelli M, Sicurelli F, Scarpini C, Dotti MT, Federico A (2001) Cerebrotendinous xanthomatosis: 11-year treatment with chenodeoxycholic acid in five patients. An electrophysiological study. J Neurol Sci 190:29–33CrossRefPubMed
go back to reference Nicholls Z, Hobson E, Martindale J, Shaw PJ (2015) Diagnosis of spinal xanthomatosis by next-generation sequencing: identifying a rare, treatable mimic of hereditary spastic paraparesis. Pract Neurol 15:280–283CrossRefPubMed Nicholls Z, Hobson E, Martindale J, Shaw PJ (2015) Diagnosis of spinal xanthomatosis by next-generation sequencing: identifying a rare, treatable mimic of hereditary spastic paraparesis. Pract Neurol 15:280–283CrossRefPubMed
go back to reference Nie S, Chen G, Cao X, Zhang Y (2014) Cerebrotendinous xanthomatosis: a comprehensive review of pathogenesis, clinical manifestations, diagnosis, and management. Orphanet J Rare Dis 9:179CrossRefPubMedPubMedCentral Nie S, Chen G, Cao X, Zhang Y (2014) Cerebrotendinous xanthomatosis: a comprehensive review of pathogenesis, clinical manifestations, diagnosis, and management. Orphanet J Rare Dis 9:179CrossRefPubMedPubMedCentral
go back to reference Panzenboeck U, Andersson U, Hansson M, Sattler W, Meaney S, Björkhem I (2007) On the mechanism of cerebral accumulation of cholestanol in patients with cerebrotendinous xanthomatosis. J Lipid Res 48:1167–1174CrossRefPubMed Panzenboeck U, Andersson U, Hansson M, Sattler W, Meaney S, Björkhem I (2007) On the mechanism of cerebral accumulation of cholestanol in patients with cerebrotendinous xanthomatosis. J Lipid Res 48:1167–1174CrossRefPubMed
go back to reference Peynet J, Laurent A, De Liege P et al (1991) Cerebrotendinous xanthomatosis: treatments with simvastatin, lovastatin, and chenodeoxycholic acid in 3 siblings. Neurology 41:434–436CrossRefPubMed Peynet J, Laurent A, De Liege P et al (1991) Cerebrotendinous xanthomatosis: treatments with simvastatin, lovastatin, and chenodeoxycholic acid in 3 siblings. Neurology 41:434–436CrossRefPubMed
go back to reference Pilo de la Fuente B, Ruiz I, Lopez de Munain A, Jimenez-Escrig A (2008) Cerebrotendinous xanthomatosis: neuropathological findings. J Neurol 255:839–842CrossRefPubMed Pilo de la Fuente B, Ruiz I, Lopez de Munain A, Jimenez-Escrig A (2008) Cerebrotendinous xanthomatosis: neuropathological findings. J Neurol 255:839–842CrossRefPubMed
go back to reference Pilo-de-la-Fuente B, Jimenez-Escrig A, Lorenzo JR et al (2011) Cerebrotendinous xanthomatosis in Spain: clinical, prognostic, and genetic survey. Eur J Neurol 18:1203–1211CrossRefPubMed Pilo-de-la-Fuente B, Jimenez-Escrig A, Lorenzo JR et al (2011) Cerebrotendinous xanthomatosis in Spain: clinical, prognostic, and genetic survey. Eur J Neurol 18:1203–1211CrossRefPubMed
go back to reference Rosafio F, Cavallieri F, Guaraldi P, Taroni F, Nichelli PF, Mandrioli J (2016) The wide spectrum of cerebrotendinous xanthomatosis: case report of a rare but treatable disease. Clin Neurol Neurosurg 143:1–3CrossRefPubMed Rosafio F, Cavallieri F, Guaraldi P, Taroni F, Nichelli PF, Mandrioli J (2016) The wide spectrum of cerebrotendinous xanthomatosis: case report of a rare but treatable disease. Clin Neurol Neurosurg 143:1–3CrossRefPubMed
go back to reference Rosen H, Reshef A, Maeda N et al (1998) Markedly reduced bile acid synthesis but maintained levels of cholesterol and vitamin D metabolites in mice with disrupted sterol 27-hydroxylase gene. J Biol Chem 273:14805–14812CrossRefPubMed Rosen H, Reshef A, Maeda N et al (1998) Markedly reduced bile acid synthesis but maintained levels of cholesterol and vitamin D metabolites in mice with disrupted sterol 27-hydroxylase gene. J Biol Chem 273:14805–14812CrossRefPubMed
go back to reference Rosner G, Rosner S, Orr-Urtreger A (2009) Genetic testing in Israel: an overview. Annu Rev Genomics Hum Genet 10:175–192CrossRefPubMed Rosner G, Rosner S, Orr-Urtreger A (2009) Genetic testing in Israel: an overview. Annu Rev Genomics Hum Genet 10:175–192CrossRefPubMed
go back to reference Salen G (1971) Cholestanol deposition in cerebrotendinous xanthomatosis. A possible mechanism. Ann Intern Med 75:843–851CrossRefPubMed Salen G (1971) Cholestanol deposition in cerebrotendinous xanthomatosis. A possible mechanism. Ann Intern Med 75:843–851CrossRefPubMed
go back to reference Salen G, Meriwether TW, Nicolau G (1975) Chenodeoxycholic acid inhibits increased cholesterol and cholestanol synthesis in patients with cerebrotendinous xanthomatosis. Biochem Med 14:57–74CrossRefPubMed Salen G, Meriwether TW, Nicolau G (1975) Chenodeoxycholic acid inhibits increased cholesterol and cholestanol synthesis in patients with cerebrotendinous xanthomatosis. Biochem Med 14:57–74CrossRefPubMed
go back to reference Salen G, Kwiterovich PO Jr, Shefer S et al (1985) Increased plasma cholestanol and 5α-saturated plant sterol derivatives in subjects with sitosterolemia and xanthomatosis. J Lipid Res 26:203–209PubMed Salen G, Kwiterovich PO Jr, Shefer S et al (1985) Increased plasma cholestanol and 5α-saturated plant sterol derivatives in subjects with sitosterolemia and xanthomatosis. J Lipid Res 26:203–209PubMed
go back to reference Salen G, Berginer V, Shore V et al (1987) Increased concentrations of cholestanol and apolipoprotein B in the cerebrospinal fluid of patients with cerebrotendinous xanthomatosis. Effect of chenodeoxycholic acid. N Engl J Med 316:1233–1238CrossRefPubMed Salen G, Berginer V, Shore V et al (1987) Increased concentrations of cholestanol and apolipoprotein B in the cerebrospinal fluid of patients with cerebrotendinous xanthomatosis. Effect of chenodeoxycholic acid. N Engl J Med 316:1233–1238CrossRefPubMed
go back to reference Salen G, Shefer S, Berginer V (1991) Biochemical abnormalities in cerebrotendinous xanthomatosis. Dev Neurosci 13:363–370CrossRefPubMed Salen G, Shefer S, Berginer V (1991) Biochemical abnormalities in cerebrotendinous xanthomatosis. Dev Neurosci 13:363–370CrossRefPubMed
go back to reference Salen G, Batta AK, Tint GS, Shefer S (1994) Comparative effects of lovastatin and chenodeoxycholic acid on plasma cholestanol levels and abnormal bile acid metabolism in cerebrotendinous xanthomatosis. Metabolism 43:1018–1022CrossRefPubMed Salen G, Batta AK, Tint GS, Shefer S (1994) Comparative effects of lovastatin and chenodeoxycholic acid on plasma cholestanol levels and abnormal bile acid metabolism in cerebrotendinous xanthomatosis. Metabolism 43:1018–1022CrossRefPubMed
go back to reference Saute JA, Giugliani R, Merkens LS, Chiang JP, DeBarber AE, de Souza CF (2015) Look carefully to the heels! A potentially treatable cause of spastic paraplegia. J Inherit Metab Dis 38:363–364CrossRefPubMed Saute JA, Giugliani R, Merkens LS, Chiang JP, DeBarber AE, de Souza CF (2015) Look carefully to the heels! A potentially treatable cause of spastic paraplegia. J Inherit Metab Dis 38:363–364CrossRefPubMed
go back to reference Stelten BML, Verrips A, Bonnot O, Huidekoper HH, Kluijtmans LAJ, Wevers RA (2017) Austism spectrum disorder in cerebrotendinous anthomatosis. Neurology 88(suppl) Stelten BML, Verrips A, Bonnot O, Huidekoper HH, Kluijtmans LAJ, Wevers RA (2017) Austism spectrum disorder in cerebrotendinous anthomatosis. Neurology 88(suppl)
go back to reference Theofilopoulos S, Griffiths WJ, Crick PJ et al (2014) Cholestenoic acids regulate motor neuron survival via liver X receptors. J Clin Invest 124:4829–4842CrossRefPubMedPubMedCentral Theofilopoulos S, Griffiths WJ, Crick PJ et al (2014) Cholestenoic acids regulate motor neuron survival via liver X receptors. J Clin Invest 124:4829–4842CrossRefPubMedPubMedCentral
go back to reference Tint GS, Ginsberg H, Salen G, Le NA, Shefer S (1989) Chenodeoxycholic acid normalizes elevated lipoprotein secretion and catabolism in cerebrotendinous xanthomatosis. J Lipid Res 30:633–640PubMed Tint GS, Ginsberg H, Salen G, Le NA, Shefer S (1989) Chenodeoxycholic acid normalizes elevated lipoprotein secretion and catabolism in cerebrotendinous xanthomatosis. J Lipid Res 30:633–640PubMed
go back to reference Tokimura Y, Kuriyama M, Arimura K, Fujiyama J, Osame M (1992) Electrophysiological studies in cerebrotendinous xanthomatosis. J Neurol Neurosurg Psychiatry 55:52–55CrossRefPubMedPubMedCentral Tokimura Y, Kuriyama M, Arimura K, Fujiyama J, Osame M (1992) Electrophysiological studies in cerebrotendinous xanthomatosis. J Neurol Neurosurg Psychiatry 55:52–55CrossRefPubMedPubMedCentral
go back to reference Valdivielso P, Calandra S, Duran JC, Garuti R, Herrera E, Gonzalez P (2004) Coronary heart disease in a patient with cerebrotendinous xanthomatosis. J Intern Med 255:680–683CrossRefPubMed Valdivielso P, Calandra S, Duran JC, Garuti R, Herrera E, Gonzalez P (2004) Coronary heart disease in a patient with cerebrotendinous xanthomatosis. J Intern Med 255:680–683CrossRefPubMed
go back to reference van Heijst AF, Verrips A, Wevers RA, Cruysberg JR, Renier WO, Tolboom JJ (1998) Treatment and follow-up of children with cerebrotendinous xanthomatosis. Eur J Pediatr 157:313–316CrossRefPubMed van Heijst AF, Verrips A, Wevers RA, Cruysberg JR, Renier WO, Tolboom JJ (1998) Treatment and follow-up of children with cerebrotendinous xanthomatosis. Eur J Pediatr 157:313–316CrossRefPubMed
go back to reference Varman KM, Dunbar K, Usifo K, Stevens CA (2016) Cerebrotendinous xanthomatosis: a treatable genetic disease not to be missed. J Clin Rheumatol 22:92–93CrossRefPubMed Varman KM, Dunbar K, Usifo K, Stevens CA (2016) Cerebrotendinous xanthomatosis: a treatable genetic disease not to be missed. J Clin Rheumatol 22:92–93CrossRefPubMed
go back to reference Vaz FM, Ferdinandusse S (2017) Bile acid analysis in human disorders of bile acid biosynthesis. Mol Asp Med 56:10–24CrossRef Vaz FM, Ferdinandusse S (2017) Bile acid analysis in human disorders of bile acid biosynthesis. Mol Asp Med 56:10–24CrossRef
go back to reference Vaz FM, Bootsma AH, Kulik W et al (2017) A newborn screening method for cerebrotendinous xanthomatosis using bile alcohol glucuronides and metabolite ratios. J Lipid Res 58:1002–1007CrossRefPubMed Vaz FM, Bootsma AH, Kulik W et al (2017) A newborn screening method for cerebrotendinous xanthomatosis using bile alcohol glucuronides and metabolite ratios. J Lipid Res 58:1002–1007CrossRefPubMed
go back to reference Verrips A, Nijeholt GJ, Barkhof F et al (1999a) Spinal xanthomatosis: a variant of cerebrotendinous xanthomatosis. Brain 122(Pt 8):1589–1595CrossRefPubMed Verrips A, Nijeholt GJ, Barkhof F et al (1999a) Spinal xanthomatosis: a variant of cerebrotendinous xanthomatosis. Brain 122(Pt 8):1589–1595CrossRefPubMed
go back to reference Verrips A, Wevers RA, van Engelen BG et al (1999b) Effect of simvastatin in addition to chenodeoxycholic acid in patients with cerebrotendinous xanthomatosis. Metabolism 48:233–238CrossRefPubMed Verrips A, Wevers RA, van Engelen BG et al (1999b) Effect of simvastatin in addition to chenodeoxycholic acid in patients with cerebrotendinous xanthomatosis. Metabolism 48:233–238CrossRefPubMed
go back to reference Verrips A, Hoefsloot LH, Steenbergen GC et al (2000a) Clinical and molecular genetic characteristics of patients with cerebrotendinous xanthomatosis. Brain 123(Pt 5):908–919CrossRefPubMed Verrips A, Hoefsloot LH, Steenbergen GC et al (2000a) Clinical and molecular genetic characteristics of patients with cerebrotendinous xanthomatosis. Brain 123(Pt 5):908–919CrossRefPubMed
go back to reference Verrips A, van Engelen BG, ter Laak H et al (2000b) Cerebrotendinous xanthomatosis. Controversies about nerve and muscle: observations in ten patients. Neuromuscul Disord 10:407–414CrossRefPubMed Verrips A, van Engelen BG, ter Laak H et al (2000b) Cerebrotendinous xanthomatosis. Controversies about nerve and muscle: observations in ten patients. Neuromuscul Disord 10:407–414CrossRefPubMed
go back to reference Verrips A, van Engelen BG, Wevers RA et al (2000c) Presence of diarrhea and absence of tendon xanthomas in patients with cerebrotendinous xanthomatosis. Arch Neurol 57:520–524CrossRefPubMed Verrips A, van Engelen BG, Wevers RA et al (2000c) Presence of diarrhea and absence of tendon xanthomas in patients with cerebrotendinous xanthomatosis. Arch Neurol 57:520–524CrossRefPubMed
go back to reference von Bahr S, Björkhem I, Van't Hooft F et al (2005) Mutation in the sterol 27-hydroxylase gene associated with fatal cholestasis in infancy. J Pediatr Gastroenterol Nutr 40:481–486CrossRef von Bahr S, Björkhem I, Van't Hooft F et al (2005) Mutation in the sterol 27-hydroxylase gene associated with fatal cholestasis in infancy. J Pediatr Gastroenterol Nutr 40:481–486CrossRef
go back to reference Waterreus RJ, Koopman BJ, Wolthers BG, Oosterhuis HJ (1987) Cerebrotendinous xanthomatosis (CTX): a clinical survey of the patient population in The Netherlands. Clin Neurol Neurosurg 89:169–175CrossRefPubMed Waterreus RJ, Koopman BJ, Wolthers BG, Oosterhuis HJ (1987) Cerebrotendinous xanthomatosis (CTX): a clinical survey of the patient population in The Netherlands. Clin Neurol Neurosurg 89:169–175CrossRefPubMed
go back to reference Yahalom G, Tsabari R, Molshatzki N, Ephraty L, Cohen H, Hassin-Baer S (2013) Neurological outcome in cerebrotendinous xanthomatosis treated with chenodeoxycholic acid: early versus late diagnosis. Clin Neuropharmacol 36:78–83CrossRefPubMed Yahalom G, Tsabari R, Molshatzki N, Ephraty L, Cohen H, Hassin-Baer S (2013) Neurological outcome in cerebrotendinous xanthomatosis treated with chenodeoxycholic acid: early versus late diagnosis. Clin Neuropharmacol 36:78–83CrossRefPubMed
go back to reference Yoshinaga T, Sekijima Y, Koyama S et al (2014) Clinical and radiological findings of a cerebrotendinous xanthomatosis patient with a novel p.A335V mutation in the CYP27A1 gene. Intern Med 53:2725–2729CrossRefPubMed Yoshinaga T, Sekijima Y, Koyama S et al (2014) Clinical and radiological findings of a cerebrotendinous xanthomatosis patient with a novel p.A335V mutation in the CYP27A1 gene. Intern Med 53:2725–2729CrossRefPubMed
go back to reference Zadori D, Szpisjak L, Madar L et al (2017) Different phenotypes in identical twins with cerebrotendinous xanthomatosis: case series. Neurol Sci 38:481–483CrossRefPubMed Zadori D, Szpisjak L, Madar L et al (2017) Different phenotypes in identical twins with cerebrotendinous xanthomatosis: case series. Neurol Sci 38:481–483CrossRefPubMed
Metadata
Title
Epidemiology, diagnosis, and treatment of cerebrotendinous xanthomatosis (CTX)
Authors
Gerald Salen
Robert D. Steiner
Publication date
01-11-2017
Publisher
Springer Netherlands
Published in
Journal of Inherited Metabolic Disease / Issue 6/2017
Print ISSN: 0141-8955
Electronic ISSN: 1573-2665
DOI
https://doi.org/10.1007/s10545-017-0093-8

Other articles of this Issue 6/2017

Journal of Inherited Metabolic Disease 6/2017 Go to the issue

Highlights

News and views

Live Webinar | 27-06-2024 | 18:00 (CEST)

Keynote webinar | Spotlight on medication adherence

Live: Thursday 27th June 2024, 18:00-19:30 (CEST)

WHO estimates that half of all patients worldwide are non-adherent to their prescribed medication. The consequences of poor adherence can be catastrophic, on both the individual and population level.

Join our expert panel to discover why you need to understand the drivers of non-adherence in your patients, and how you can optimize medication adherence in your clinics to drastically improve patient outcomes.

Prof. Kevin Dolgin
Prof. Florian Limbourg
Prof. Anoop Chauhan
Developed by: Springer Medicine
Obesity Clinical Trial Summary

At a glance: The STEP trials

A round-up of the STEP phase 3 clinical trials evaluating semaglutide for weight loss in people with overweight or obesity.

Developed by: Springer Medicine

Highlights from the ACC 2024 Congress

Year in Review: Pediatric cardiology

Watch Dr. Anne Marie Valente present the last year's highlights in pediatric and congenital heart disease in the official ACC.24 Year in Review session.

Year in Review: Pulmonary vascular disease

The last year's highlights in pulmonary vascular disease are presented by Dr. Jane Leopold in this official video from ACC.24.

Year in Review: Valvular heart disease

Watch Prof. William Zoghbi present the last year's highlights in valvular heart disease from the official ACC.24 Year in Review session.

Year in Review: Heart failure and cardiomyopathies

Watch this official video from ACC.24. Dr. Biykem Bozkurt discusses last year's major advances in heart failure and cardiomyopathies.