Skip to main content
Top
Published in: European Journal of Pediatrics 7/2016

Open Access 01-07-2016 | Original Article

Occurrence of subdural hematomas in Dutch glutaric aciduria type 1 patients

Authors: Marloes E.M. Vester, Gepke Visser, Frits A. Wijburg, Francjan J. van Spronsen, Monique Williams, Rick R. van Rijn

Published in: European Journal of Pediatrics | Issue 7/2016

Login to get access

Abstract

Patients with glutaric aciduria type 1 (GA1), a rare inherited metabolic disorder, have an increased risk for subdural hematomas (SDHs). GA1 is therefore generally included in the differential diagnosis of children presenting with SDHs. This retrospective cohort study reviews all 25 registered, in the Dutch Diagnosis Registration for Metabolic Disorders, GA1 patients in the Netherlands. This was done between May 2014 and November 2014 to determine the lifetime incidence of SDHs in this population. Seventeen patients were diagnosed either due to clinical symptoms or because of family members with GA1. One out of these 17 had a SDH. This patient showed widened Sylvian fissures on MRI, characteristic for GA1. Eight patients were diagnosed by newborn screening. Three of them had neuroimaging results, and none of them had SDHs. This study shows an overall lower incidence (4.0 %) of SDHs in patients with GA1 than reported in the literature (20–30 %).
Conclusion: This finding, in combination with the fact that SDHs in GA1 appear to occur only in the presence of characteristic brain abnormalities on imaging, we recommend that GA1 should not routinely be a part of the differential diagnosis of children with unexplained SDHs in the absence of imaging characteristics suggestive of GA1.
What is known:
Glutaric aciduria type 1 is a rare metabolic disorder predisposing children to subdural hematoma development due to brain abnormalities.
Because of these subdural hematomas, glutaric aciduria type 1 testing is part of abusive head trauma work-up.
What is new:
The overall subdural hematoma incidence in glutaric aciduria type 1 patients is much lower than previously reported and only occurs in case of predisposing brain abnormalities.
Literature
1.
go back to reference Desai NK, Runge VM, Crisp DE, Crisp MB, Naul LG (2003) Magnetic resonance imaging of the brain in glutaric acidemia type I: a review of the literature and a report of four new cases with attention to the basal ganglia and imaging technique. Investig Radiol 38:489–496. doi:10.1097/01.rli.0000080405.62988.f6 Desai NK, Runge VM, Crisp DE, Crisp MB, Naul LG (2003) Magnetic resonance imaging of the brain in glutaric acidemia type I: a review of the literature and a report of four new cases with attention to the basal ganglia and imaging technique. Investig Radiol 38:489–496. doi:10.​1097/​01.​rli.​0000080405.​62988.​f6
3.
go back to reference Fanconi M, Lips U (2010) Shaken baby syndrome in Switzerland: results of a prospective follow-up study, 2002–2007. Eur J Pediatr 169:1023–1028CrossRefPubMed Fanconi M, Lips U (2010) Shaken baby syndrome in Switzerland: results of a prospective follow-up study, 2002–2007. Eur J Pediatr 169:1023–1028CrossRefPubMed
4.
go back to reference Garbade SF, Greenberg CR, Demirkol M, Gokcay G, Ribes A, Campistol J, Burlina AB, Burgard P, Kolker S (2014) Unravelling the complex MRI pattern in glutaric aciduria type I using statistical models—a cohort study in 180 patients. J Inherit Metab Dis. doi:10.1007/s10545-014-9676-9 PubMed Garbade SF, Greenberg CR, Demirkol M, Gokcay G, Ribes A, Campistol J, Burlina AB, Burgard P, Kolker S (2014) Unravelling the complex MRI pattern in glutaric aciduria type I using statistical models—a cohort study in 180 patients. J Inherit Metab Dis. doi:10.​1007/​s10545-014-9676-9 PubMed
5.
go back to reference Harting I, Neumaier-Probst E, Seitz A, Maier EM, Assmann B, Baric I, Troncoso M, Muhlhausen C, Zschocke J, Boy NP, Hoffmann GF, Garbade SF, Kolker S (2009) Dynamic changes of striatal and extrastriatal abnormalities in glutaric aciduria type I. Brain : J Neurol 132:1764–1782. doi:10.1093/brain/awp112 CrossRef Harting I, Neumaier-Probst E, Seitz A, Maier EM, Assmann B, Baric I, Troncoso M, Muhlhausen C, Zschocke J, Boy NP, Hoffmann GF, Garbade SF, Kolker S (2009) Dynamic changes of striatal and extrastriatal abnormalities in glutaric aciduria type I. Brain : J Neurol 132:1764–1782. doi:10.​1093/​brain/​awp112 CrossRef
6.
go back to reference Hartley LM, Khwaja OS, Verity CM (2001) Glutaric aciduria type 1 and nonaccidental head injury. Pediatrics 107:174–175CrossRefPubMed Hartley LM, Khwaja OS, Verity CM (2001) Glutaric aciduria type 1 and nonaccidental head injury. Pediatrics 107:174–175CrossRefPubMed
8.
go back to reference Hoffmann GF, Athanassopoulos S, Burlina AB, Duran M, de Klerk JB, Lehnert W, Leonard JV, Monavari AA, Muller E, Muntau AC, Naughten ER, Plecko-Starting B, Superti-Furga A, Zschocke J, Christensen E (1996) Clinical course, early diagnosis, treatment, and prevention of disease in glutaryl-CoA dehydrogenase deficiency. Neuropediatrics 27:115–123. doi:10.1055/s-2007-973761 CrossRefPubMed Hoffmann GF, Athanassopoulos S, Burlina AB, Duran M, de Klerk JB, Lehnert W, Leonard JV, Monavari AA, Muller E, Muntau AC, Naughten ER, Plecko-Starting B, Superti-Furga A, Zschocke J, Christensen E (1996) Clinical course, early diagnosis, treatment, and prevention of disease in glutaryl-CoA dehydrogenase deficiency. Neuropediatrics 27:115–123. doi:10.​1055/​s-2007-973761 CrossRefPubMed
11.
go back to reference Jayawant S, Rawlinson A, Gibbon F, Price J, Schulte J, Sharples P, Sibert JR, Kemp AM (1998) Subdural haemorrhages in infants: population based study. BMJ (Clin Res Ed) 317:1558–1561CrossRef Jayawant S, Rawlinson A, Gibbon F, Price J, Schulte J, Sharples P, Sibert JR, Kemp AM (1998) Subdural haemorrhages in infants: population based study. BMJ (Clin Res Ed) 317:1558–1561CrossRef
12.
13.
go back to reference Kolker S, Christensen E, Leonard JV, Greenberg CR, Boneh A, Burlina AB, Burlina AP, Dixon M, Duran M, Garcia Cazorla A, Goodman SI, Koeller DM, Kyllerman M, Muhlhausen C, Muller E, Okun JG, Wilcken B, Hoffmann GF, Burgard P (2011) Diagnosis and management of glutaric aciduria type I—revised recommendations. J Inherit Metab Dis 34:677–694. doi:10.1007/s10545-011-9289-5 CrossRefPubMedPubMedCentral Kolker S, Christensen E, Leonard JV, Greenberg CR, Boneh A, Burlina AB, Burlina AP, Dixon M, Duran M, Garcia Cazorla A, Goodman SI, Koeller DM, Kyllerman M, Muhlhausen C, Muller E, Okun JG, Wilcken B, Hoffmann GF, Burgard P (2011) Diagnosis and management of glutaric aciduria type I—revised recommendations. J Inherit Metab Dis 34:677–694. doi:10.​1007/​s10545-011-9289-5 CrossRefPubMedPubMedCentral
14.
go back to reference Kolker S, Garbade SF, Boy N, Maier EM, Meissner T, Muhlhausen C, Hennermann JB, Lucke T, Haberle J, Baumkotter J, Haller W, Muller E, Zschocke J, Burgard P, Hoffmann GF (2007) Decline of acute encephalopathic crises in children with glutaryl-CoA dehydrogenase deficiency identified by newborn screening in Germany. Pediatr Res 62:357–363. doi:10.1203/PDR.0b013e318137a124 CrossRefPubMed Kolker S, Garbade SF, Boy N, Maier EM, Meissner T, Muhlhausen C, Hennermann JB, Lucke T, Haberle J, Baumkotter J, Haller W, Muller E, Zschocke J, Burgard P, Hoffmann GF (2007) Decline of acute encephalopathic crises in children with glutaryl-CoA dehydrogenase deficiency identified by newborn screening in Germany. Pediatr Res 62:357–363. doi:10.​1203/​PDR.​0b013e318137a124​ CrossRefPubMed
15.
go back to reference Kolker S, Garbade SF, Greenberg CR, Leonard JV, Saudubray JM, Ribes A, Kalkanoglu HS, Lund AM, Merinero B, Wajner M, Troncoso M, Williams M, Walter JH, Campistol J, Marti-Herrero M, Caswill M, Burlina AB, Lagler F, Maier EM, Schwahn B, Tokatli A, Dursun A, Coskun T, Chalmers RA, Koeller DM, Zschocke J, Christensen E, Burgard P, Hoffmann GF (2006) Natural history, outcome, and treatment efficacy in children and adults with glutaryl-CoA dehydrogenase deficiency. Pediatr Res 59:840–847. doi:10.1203/01.pdr.0000219387.79887.86 CrossRefPubMed Kolker S, Garbade SF, Greenberg CR, Leonard JV, Saudubray JM, Ribes A, Kalkanoglu HS, Lund AM, Merinero B, Wajner M, Troncoso M, Williams M, Walter JH, Campistol J, Marti-Herrero M, Caswill M, Burlina AB, Lagler F, Maier EM, Schwahn B, Tokatli A, Dursun A, Coskun T, Chalmers RA, Koeller DM, Zschocke J, Christensen E, Burgard P, Hoffmann GF (2006) Natural history, outcome, and treatment efficacy in children and adults with glutaryl-CoA dehydrogenase deficiency. Pediatr Res 59:840–847. doi:10.​1203/​01.​pdr.​0000219387.​79887.​86 CrossRefPubMed
17.
go back to reference Lin S, Hsu S, Ho E, Tsai C, Hseih Y, Lo F, Lai H, Chen M (2002) Novel mutation and prenatal sonographic findings of glutaric aciduria (type I) in two Taiwanese families. Prenat Diagn 22:725–729CrossRefPubMed Lin S, Hsu S, Ho E, Tsai C, Hseih Y, Lo F, Lai H, Chen M (2002) Novel mutation and prenatal sonographic findings of glutaric aciduria (type I) in two Taiwanese families. Prenat Diagn 22:725–729CrossRefPubMed
19.
go back to reference Mellerio C, Marignier S, Roth P, Gaucherand P, Des Portes V, Pracros J, Guibaud L (2008) Prenatal cerebral ultrasound and MRI findings in glutaric aciduria Type 1: a de novo case. Ultrasound Obstet Gynecol 31:712–714CrossRefPubMed Mellerio C, Marignier S, Roth P, Gaucherand P, Des Portes V, Pracros J, Guibaud L (2008) Prenatal cerebral ultrasound and MRI findings in glutaric aciduria Type 1: a de novo case. Ultrasound Obstet Gynecol 31:712–714CrossRefPubMed
20.
go back to reference Osaka H, Kimura S, Nezu A, Yamazaki S, Saitoh K, Yamaguchi S (1993) Chronic subdural hematoma, as an initial manifestation of glutaric aciduria type-1. Brain Dev 15:125–127CrossRefPubMed Osaka H, Kimura S, Nezu A, Yamazaki S, Saitoh K, Yamaguchi S (1993) Chronic subdural hematoma, as an initial manifestation of glutaric aciduria type-1. Brain Dev 15:125–127CrossRefPubMed
21.
go back to reference Sieswerda-Hoogendoorn T, Boos S, Spivack B, Bilo RA, van Rijn RR (2012) Educational paper. Eur J Pediatr 171:415–423CrossRefPubMed Sieswerda-Hoogendoorn T, Boos S, Spivack B, Bilo RA, van Rijn RR (2012) Educational paper. Eur J Pediatr 171:415–423CrossRefPubMed
22.
23.
go back to reference Strauss KA, Puffenberger EG, Robinson DL, Morton DH, Strauss KA, Puffenberger EG, Robinson DL, Morton DH (2003) Type I glutaric aciduria, part 1: natural history of 77 patients. Am J Med Genet C Semin Med Genet 121c:38–52. doi:10.1002/ajmg.c.20007 CrossRefPubMed Strauss KA, Puffenberger EG, Robinson DL, Morton DH, Strauss KA, Puffenberger EG, Robinson DL, Morton DH (2003) Type I glutaric aciduria, part 1: natural history of 77 patients. Am J Med Genet C Semin Med Genet 121c:38–52. doi:10.​1002/​ajmg.​c.​20007 CrossRefPubMed
26.
go back to reference Woelfle J, Kreft B, Emons D, Haverkamp F (1996) Subdural hemorrhage as an initial sign of glutaric aciduria type 1: a diagnostic pitfall. Pediatr Radiol 26:779–781CrossRefPubMed Woelfle J, Kreft B, Emons D, Haverkamp F (1996) Subdural hemorrhage as an initial sign of glutaric aciduria type 1: a diagnostic pitfall. Pediatr Radiol 26:779–781CrossRefPubMed
Metadata
Title
Occurrence of subdural hematomas in Dutch glutaric aciduria type 1 patients
Authors
Marloes E.M. Vester
Gepke Visser
Frits A. Wijburg
Francjan J. van Spronsen
Monique Williams
Rick R. van Rijn
Publication date
01-07-2016
Publisher
Springer Berlin Heidelberg
Published in
European Journal of Pediatrics / Issue 7/2016
Print ISSN: 0340-6199
Electronic ISSN: 1432-1076
DOI
https://doi.org/10.1007/s00431-016-2734-6

Other articles of this Issue 7/2016

European Journal of Pediatrics 7/2016 Go to the issue