Skip to main content
Top
Published in: Journal of Genetic Counseling 5/2013

01-10-2013 | PROFESSIONAL ISSUES

Fabry Disease Practice Guidelines: Recommendations of the National Society of Genetic Counselors

Authors: Dawn A. Laney, Robin L. Bennett, Virginia Clarke, Angela Fox, Robert J. Hopkin, Jack Johnson, Erin O’Rourke, Katherine Sims, Gerald Walter

Published in: Journal of Genetic Counseling | Issue 5/2013

Login to get access

Abstract

Identification and comprehensive care of individuals who have Fabry disease (FD) requires a multidisciplinary approach inclusive of genetic testing, test interpretation, genetic counseling, long term disease symptom monitoring, treatment recommendations, and coordination of therapy. The purpose of this document is to provide health care professionals with guidelines for testing, care coordination, identification of psychosocial issues, and to facilitate a better understanding of disease treatment expert recommendations for patients with Fabry disease. These recommendations are the opinions of a multicenter working group of genetic counselors, medical geneticists, and other health professionals with expertise in Fabry disease counseling, as well as representatives/founders of the two United States based Fabry disease patient advocacy groups who are themselves affected by Fabry disease. The recommendations are U.S. Preventive Task Force Class III, and they are based on clinical experience, a review of pertinent English-language articles, and reports of expert committees. This document reviews the genetics of Fabry disease, the indications for genetic testing, interpretation of results, psychosocial considerations, and references to professional and patient resources.
Literature
go back to reference Abe, A., Gregory, S., Lee, L., Killen, P. D., Brady, R. O., Kulkarni, A., et al. (2000). Reduction of globotriaosylceramide in Fabry disease mice by substrate deprivation. The Journal of Clinical Investigation, 105, 1563–1571.PubMedCrossRef Abe, A., Gregory, S., Lee, L., Killen, P. D., Brady, R. O., Kulkarni, A., et al. (2000). Reduction of globotriaosylceramide in Fabry disease mice by substrate deprivation. The Journal of Clinical Investigation, 105, 1563–1571.PubMedCrossRef
go back to reference Albano, L. M., Rivitti, C., Bertola, D. R., Honjo, R. S., Kelmann, S. V., Giugliana, R., et al. (2010). Angiokeratoma: a cutaneous marker of Fabry’s disease. Clinical and Experimental Dermatology, 35(5), 505–508.PubMedCrossRef Albano, L. M., Rivitti, C., Bertola, D. R., Honjo, R. S., Kelmann, S. V., Giugliana, R., et al. (2010). Angiokeratoma: a cutaneous marker of Fabry’s disease. Clinical and Experimental Dermatology, 35(5), 505–508.PubMedCrossRef
go back to reference Ashton-Prolla, P., Tong, B., Shabeer, J., Eng, C. M., & Desnick, R. J. (2000). 22 novel mutations in the alpha-galactosidase A gene and genotype/phenotype correlations including mild hemizygotes and severely affected heterozygotes. Journal of Investigative Medicine, 48, 227.PubMed Ashton-Prolla, P., Tong, B., Shabeer, J., Eng, C. M., & Desnick, R. J. (2000). 22 novel mutations in the alpha-galactosidase A gene and genotype/phenotype correlations including mild hemizygotes and severely affected heterozygotes. Journal of Investigative Medicine, 48, 227.PubMed
go back to reference Banikazemi, M., Bultas, J., Waldek, S., Wilcox, W. R., Whitley, C. B., McDonald, M., et al. (2007). Agalsidase-beta therapy for advanced Fabry disease: a randomized trial. Annals of Internal Medicine, 146(2), 77–86.PubMedCrossRef Banikazemi, M., Bultas, J., Waldek, S., Wilcox, W. R., Whitley, C. B., McDonald, M., et al. (2007). Agalsidase-beta therapy for advanced Fabry disease: a randomized trial. Annals of Internal Medicine, 146(2), 77–86.PubMedCrossRef
go back to reference Bennett, R. L. (2010a). The practical guide to the genetic family history (2nd ed.). Hoboken: Blackwell.CrossRef Bennett, R. L. (2010a). The practical guide to the genetic family history (2nd ed.). Hoboken: Blackwell.CrossRef
go back to reference Bennett, R. L. (2010b). Genetic counseling and psychosocial issues for individuals and their families with Fabry disease. In Elstein D, Altarescu G, Beck M (Eds.), Fabry disease. New York: Springer. Bennett, R. L. (2010b). Genetic counseling and psychosocial issues for individuals and their families with Fabry disease. In Elstein D, Altarescu G, Beck M (Eds.), Fabry disease. New York: Springer.
go back to reference Bennett, R. L., Steinhaus, K. A., Uhrich, S. B., O’Sullivan, C. K., Resta, R. G., Lochner-Doyle, D., et al. (1995). Recommendations for standardized pedigree nomenclature. American Journal of Human Genetics, 56, 745–752.PubMed Bennett, R. L., Steinhaus, K. A., Uhrich, S. B., O’Sullivan, C. K., Resta, R. G., Lochner-Doyle, D., et al. (1995). Recommendations for standardized pedigree nomenclature. American Journal of Human Genetics, 56, 745–752.PubMed
go back to reference Bennett, R. L., Hart, K. A., O’Rourke, E. O., et al. (2002). Fabry disease in genetic counseling practice: recommendations of the National Society of Genetic Counselors. Journal of Genetic Counseling, 11(2), 121–146.PubMedCrossRef Bennett, R. L., Hart, K. A., O’Rourke, E. O., et al. (2002). Fabry disease in genetic counseling practice: recommendations of the National Society of Genetic Counselors. Journal of Genetic Counseling, 11(2), 121–146.PubMedCrossRef
go back to reference Bennett, R. L., Steinhaus, K. A., Resta, R. G., & Doyle, D. L. (2008). Standardized human pedigree nomenclature: update and assessment of the recommendations of the National Society of Genetic Counselors. Journal of Genetic Counseling, 7(5), 424–433.CrossRef Bennett, R. L., Steinhaus, K. A., Resta, R. G., & Doyle, D. L. (2008). Standardized human pedigree nomenclature: update and assessment of the recommendations of the National Society of Genetic Counselors. Journal of Genetic Counseling, 7(5), 424–433.CrossRef
go back to reference Brady, R. O., & Schiffmann, R. (2000). Clinical features of and recent advances in therapy for Fabry disease. Journal of the American Medical Association, 284, 2771–2775.PubMedCrossRef Brady, R. O., & Schiffmann, R. (2000). Clinical features of and recent advances in therapy for Fabry disease. Journal of the American Medical Association, 284, 2771–2775.PubMedCrossRef
go back to reference Brower, A., Hoffman, A. J., Thompson, B. H, & Watson, M. S. (2011). Utilization of the newborn screening translational research network to advance research and clinical applications in lysosomal storage disorders. 7th WORLD symposium 2011. Brower, A., Hoffman, A. J., Thompson, B. H, & Watson, M. S. (2011). Utilization of the newborn screening translational research network to advance research and clinical applications in lysosomal storage disorders. 7th WORLD symposium 2011.
go back to reference Chimenti, C., Pieroni, M., Morgante, E., et al. (2004). Prevalaence of Fabry disease in female patients with late-onset hypertrophic cardiomyopathy. Circulation, 110(9), 1047–1053. Epub 2004 Aug 16.PubMedCrossRef Chimenti, C., Pieroni, M., Morgante, E., et al. (2004). Prevalaence of Fabry disease in female patients with late-onset hypertrophic cardiomyopathy. Circulation, 110(9), 1047–1053. Epub 2004 Aug 16.PubMedCrossRef
go back to reference Clarke, A. (Ed.). (1998). The genetic testing of children. Oxford: BIOS Scientific. Clarke, A. (Ed.). (1998). The genetic testing of children. Oxford: BIOS Scientific.
go back to reference Clarke, A., & Flinter, F. (1996). The genetic testing of children: A clinical perspective. In T. Marteau & M. Richards (Eds.), The troubled helix: Social and psychological implications of the new human genetics (pp. 164–176). New York: Cambridge University Press.CrossRef Clarke, A., & Flinter, F. (1996). The genetic testing of children: A clinical perspective. In T. Marteau & M. Richards (Eds.), The troubled helix: Social and psychological implications of the new human genetics (pp. 164–176). New York: Cambridge University Press.CrossRef
go back to reference Colombi, A., Kostyal, A., Bracher, R., Gloor, F., Mazzi, R., & Tholen, H. (1967). Angiokeratoma corporis diffusum: Fabry’s disease. Helvetica Medica Acta, 34, 67–83.PubMed Colombi, A., Kostyal, A., Bracher, R., Gloor, F., Mazzi, R., & Tholen, H. (1967). Angiokeratoma corporis diffusum: Fabry’s disease. Helvetica Medica Acta, 34, 67–83.PubMed
go back to reference Davis, D. S. (1997). Genetic dilemmas and the child’s right to an open future. The Hastings Center Report, 27, 7–15.PubMedCrossRef Davis, D. S. (1997). Genetic dilemmas and the child’s right to an open future. The Hastings Center Report, 27, 7–15.PubMedCrossRef
go back to reference Desnick, R. J. (2004). Enzyme replacement therapy for Fabry disease: lessons from two alpha-galactosidase A orphan products and one FDA approval. Expert Opinion on Biological Therapy, 4, 1167–1176.PubMedCrossRef Desnick, R. J. (2004). Enzyme replacement therapy for Fabry disease: lessons from two alpha-galactosidase A orphan products and one FDA approval. Expert Opinion on Biological Therapy, 4, 1167–1176.PubMedCrossRef
go back to reference Desnick, R., & Ioannou, Y., (2006). Eng C. α-Galactosidase A deficiency: Fabry disease. In: Valle D, Baudette A, Vogelstein KC, (Eds.), The online metabolic & molecular bases of inherited disease. McGraw-Hill Companies Inc. www.ommbid.com, accessed Mar 2011. Desnick, R., & Ioannou, Y., (2006). Eng C. α-Galactosidase A deficiency: Fabry disease. In: Valle D, Baudette A, Vogelstein KC, (Eds.), The online metabolic & molecular bases of inherited disease. McGraw-Hill Companies Inc. www.​ommbid.​com, accessed Mar 2011.
go back to reference Desnick, R. J., Brady, R., Barranger, J., et al. (2003). Fabry disease, an under-recognized multisystemic disorder: expert recommendations for diagnosis, management, and enzyme replacement therapy. Annals of Internal Medicine, 138, 338–346.PubMedCrossRef Desnick, R. J., Brady, R., Barranger, J., et al. (2003). Fabry disease, an under-recognized multisystemic disorder: expert recommendations for diagnosis, management, and enzyme replacement therapy. Annals of Internal Medicine, 138, 338–346.PubMedCrossRef
go back to reference Dink, A., Sims, I., Pay, S., Calgary, K., & Can, C. (2000). Fabry’s disease mimicking familial Mediterranean fever. Clinical and Experimental Rheumatic, 18, 787–788. Dink, A., Sims, I., Pay, S., Calgary, K., & Can, C. (2000). Fabry’s disease mimicking familial Mediterranean fever. Clinical and Experimental Rheumatic, 18, 787–788.
go back to reference Elstein, D., Altars, G., & Beck, M. (ends) (2010). Fabry disease, Springer. Elstein, D., Altars, G., & Beck, M. (ends) (2010). Fabry disease, Springer.
go back to reference Eng, C. M., Banikazemi, M., Gordon, R. E., Goldman, M., Phelps, R., Kim, L., et al. (2001a). A phase 1/2 clinical trial of enzyme replacement in Fabry disease: pharmacokinetic, substrate clearance, and safety studies. American Journal of Human Genetics, 68, 711–722.PubMedCrossRef Eng, C. M., Banikazemi, M., Gordon, R. E., Goldman, M., Phelps, R., Kim, L., et al. (2001a). A phase 1/2 clinical trial of enzyme replacement in Fabry disease: pharmacokinetic, substrate clearance, and safety studies. American Journal of Human Genetics, 68, 711–722.PubMedCrossRef
go back to reference Eng, C. M., Guffon, N., Wilcox, W. R., Germain, D. P., Lee, P., Waldek, S., et al. (2001b). Safety and efficacy of recombinant human ®-galactosidase A replacement therapy in Fairy’s disease. The New England Journal of Medicine, 345, 9–16.CrossRef Eng, C. M., Guffon, N., Wilcox, W. R., Germain, D. P., Lee, P., Waldek, S., et al. (2001b). Safety and efficacy of recombinant human ®-galactosidase A replacement therapy in Fairy’s disease. The New England Journal of Medicine, 345, 9–16.CrossRef
go back to reference Eng, C. M., Germain, D. P., Banikazemi, M., Warnock, D. G., Wanner, C., Hopkin, R. J., et al. (2006). Fabry disease: guidelines for the evaluation and management of multi-organ system involvement. Genetics in Medicine, 8(9), 539–548.PubMedCrossRef Eng, C. M., Germain, D. P., Banikazemi, M., Warnock, D. G., Wanner, C., Hopkin, R. J., et al. (2006). Fabry disease: guidelines for the evaluation and management of multi-organ system involvement. Genetics in Medicine, 8(9), 539–548.PubMedCrossRef
go back to reference Gahl, W. A. (2001). New therapies for Fabry’s disease. The New England Journal of Medicine, 345, 55–57.PubMedCrossRef Gahl, W. A. (2001). New therapies for Fabry’s disease. The New England Journal of Medicine, 345, 55–57.PubMedCrossRef
go back to reference Gibas, A. L., Klatt, R., Johnson, J., Clarket, J. T. R., & Katz, J. (2008). Disease rarity, carrier status, and genera: a triple disadvantage for women with Fabry disease. Journal of Genetic Counseling, 17, 528–537.PubMedCrossRef Gibas, A. L., Klatt, R., Johnson, J., Clarket, J. T. R., & Katz, J. (2008). Disease rarity, carrier status, and genera: a triple disadvantage for women with Fabry disease. Journal of Genetic Counseling, 17, 528–537.PubMedCrossRef
go back to reference Grewal, R. P. (1993). Psychiatric disorders in patients with Fabry’s disease. International Journal of Psychiatry in Medicine, 23, 307–312.PubMedCrossRef Grewal, R. P. (1993). Psychiatric disorders in patients with Fabry’s disease. International Journal of Psychiatry in Medicine, 23, 307–312.PubMedCrossRef
go back to reference Hershberger, R. E., Lindenfeld, J., Mestroni, L., Seidman, C. E., Taylor, M. R. G., & Towbin, J. A. (2009). Journal of Cardiac Failure, 15(2), 83–97.PubMedCrossRef Hershberger, R. E., Lindenfeld, J., Mestroni, L., Seidman, C. E., Taylor, M. R. G., & Towbin, J. A. (2009). Journal of Cardiac Failure, 15(2), 83–97.PubMedCrossRef
go back to reference Holmes, L. B., Harvey, E. A., Coull, B. A., Huntington, K. B., Khoshbin, S., Hayes, A. M., et al. (2001). The teratogenicity of anticonvulsant drugs. The New England Journal of Medicine, 344, 1132–1138.PubMedCrossRef Holmes, L. B., Harvey, E. A., Coull, B. A., Huntington, K. B., Khoshbin, S., Hayes, A. M., et al. (2001). The teratogenicity of anticonvulsant drugs. The New England Journal of Medicine, 344, 1132–1138.PubMedCrossRef
go back to reference Hopkin, R. J., Bissler, J., Banikazemi, M., Clarke, L., Eng, C. M., Germain, D. P., et al. (2008). Characterization of Fabry disease in 352 pediatric patients in the Fabry Registry. Pediatric Research, 64, 550–555.PubMedCrossRef Hopkin, R. J., Bissler, J., Banikazemi, M., Clarke, L., Eng, C. M., Germain, D. P., et al. (2008). Characterization of Fabry disease in 352 pediatric patients in the Fabry Registry. Pediatric Research, 64, 550–555.PubMedCrossRef
go back to reference Laney, D. A., & Fernhoff, P. M. (2008). Diagnosis of Fabry disease via analysis of family history. Journal of Genetic Counseling, 17(1), 79–83.PubMedCrossRef Laney, D. A., & Fernhoff, P. M. (2008). Diagnosis of Fabry disease via analysis of family history. Journal of Genetic Counseling, 17(1), 79–83.PubMedCrossRef
go back to reference Laney, D.A., Gruskin, D.J., Fernhoff, P.M., Cubells, J.F., Ousley, O.Y., Hipp, H., et al. (2010). Social-adaptive and psychological functioning of patients affected by fabry disease. Journal of Inherited Metabolic Disease. Online. Laney, D.A., Gruskin, D.J., Fernhoff, P.M., Cubells, J.F., Ousley, O.Y., Hipp, H., et al. (2010). Social-adaptive and psychological functioning of patients affected by fabry disease. Journal of Inherited Metabolic Disease. Online.
go back to reference Lee, K., Jin, X., Zhang, K., Copertino, L., Andrews, L., Baker-Malcolm, J., et al. (2003). A biochemical and pharmacological comparison of enzyme replacement therapies for the glycolipid storage disorder Fabry disease. Glycobiology, 13, 305–313.PubMedCrossRef Lee, K., Jin, X., Zhang, K., Copertino, L., Andrews, L., Baker-Malcolm, J., et al. (2003). A biochemical and pharmacological comparison of enzyme replacement therapies for the glycolipid storage disorder Fabry disease. Glycobiology, 13, 305–313.PubMedCrossRef
go back to reference Lidov, O., West, M., Pintos-Morell, G., et al. (2010). Effects of enzyme replacement therapy in Fabry disease—A comprehensive review of the medical literature. Genetics in Medicine, 12(11). Lidov, O., West, M., Pintos-Morell, G., et al. (2010). Effects of enzyme replacement therapy in Fabry disease—A comprehensive review of the medical literature. Genetics in Medicine, 12(11).
go back to reference Lin, H. Y., Chong, K. W., Hsu, J. H., et al. (2009). High incidence of the cardiac variant of Fabry disease revealed by newborn screening in the Taiwan Chinese population. Circulation. Cardiovascular Genetics, 2, 450–456.PubMedCrossRef Lin, H. Y., Chong, K. W., Hsu, J. H., et al. (2009). High incidence of the cardiac variant of Fabry disease revealed by newborn screening in the Taiwan Chinese population. Circulation. Cardiovascular Genetics, 2, 450–456.PubMedCrossRef
go back to reference MacDermot, K. D., Holmes, A., & Miners, A. H. (2001a). Anderson Fabry disease: clinical manifestations and impact of disease in a cohort of 98 hemizygous males. Journal of Medical Genetics, 38, 750–760.PubMedCrossRef MacDermot, K. D., Holmes, A., & Miners, A. H. (2001a). Anderson Fabry disease: clinical manifestations and impact of disease in a cohort of 98 hemizygous males. Journal of Medical Genetics, 38, 750–760.PubMedCrossRef
go back to reference MacDermot, K. D., Holmes, A., & Miners, A. H. (2001b). Anderson Fabry disease: clinical manifestations and impact of disease in a cohort of 60 obligate carrier females. Journal of Medical Genetics, 38, 769–775.PubMedCrossRef MacDermot, K. D., Holmes, A., & Miners, A. H. (2001b). Anderson Fabry disease: clinical manifestations and impact of disease in a cohort of 60 obligate carrier females. Journal of Medical Genetics, 38, 769–775.PubMedCrossRef
go back to reference McConkie-Rosell, A., & DeVellis, B. M. (2000). Threat to parental role: a possible mechanism of altered self-concept related to carrier knowledge. Journal of Genetic Counseling, 9, 285–302.CrossRef McConkie-Rosell, A., & DeVellis, B. M. (2000). Threat to parental role: a possible mechanism of altered self-concept related to carrier knowledge. Journal of Genetic Counseling, 9, 285–302.CrossRef
go back to reference Mehta, A., Ricci, R., Widmer, U., et al. (2004). Fabry disease defined, baseline clinical manifestations of 366 patients in the Fabry outcome survey. European Journal of Clinical Investigation, 34(3), 235–242.CrossRef Mehta, A., Ricci, R., Widmer, U., et al. (2004). Fabry disease defined, baseline clinical manifestations of 366 patients in the Fabry outcome survey. European Journal of Clinical Investigation, 34(3), 235–242.CrossRef
go back to reference Mehta, A., Beck, M., & Sunder-Plassmann, G. (Eds.). (2006). Fabry disease: Perspectives from 5 years of FOS. Oxford: Oxford PharmaGenesis. Mehta, A., Beck, M., & Sunder-Plassmann, G. (Eds.). (2006). Fabry disease: Perspectives from 5 years of FOS. Oxford: Oxford PharmaGenesis.
go back to reference Meikle, P. J., Hopwood, J. J., Clague, A. E., & Carey, W. F. (1999). Prevalence of lysosomal storage disorders. Journal of the American Medical Association, 281, 249–254.PubMedCrossRef Meikle, P. J., Hopwood, J. J., Clague, A. E., & Carey, W. F. (1999). Prevalence of lysosomal storage disorders. Journal of the American Medical Association, 281, 249–254.PubMedCrossRef
go back to reference Michie, S. (1996). Predictive genetic testing in children: Paternalism or empiricisms? In T. Marteau & M. Richards (Eds.), The troubled helix: Social and psychological implications of the new human genetics (pp. 177–183). New York: Cambridge University Press.CrossRef Michie, S. (1996). Predictive genetic testing in children: Paternalism or empiricisms? In T. Marteau & M. Richards (Eds.), The troubled helix: Social and psychological implications of the new human genetics (pp. 177–183). New York: Cambridge University Press.CrossRef
go back to reference Motabar, O., Sidransky, E., Goldin, E., & Zheng, W. (2010). Fabry disease- current treatment and new drug development. Current Chemical Genomics, 4, 50–56.PubMedCrossRef Motabar, O., Sidransky, E., Goldin, E., & Zheng, W. (2010). Fabry disease- current treatment and new drug development. Current Chemical Genomics, 4, 50–56.PubMedCrossRef
go back to reference National Society of Genetic Counselors. (1995). National Society of Genetic Counselors, Position statement on prenatal and childhood testing for adult-onset disorders. Perspectives Genetic Counseling, 17, 5. National Society of Genetic Counselors. (1995). National Society of Genetic Counselors, Position statement on prenatal and childhood testing for adult-onset disorders. Perspectives Genetic Counseling, 17, 5.
go back to reference Ortiz, A., Oliveira, J. P., Waldek, S., Warnock, D. G., Cianciaruso, B., Wanner, C., et al. (2008a). Nephropathy in males and females with Fabry disease: cross-sectional description of patients before treatment with enzyme replacement therapy. Nephrology, Dialysis, Transplantation, 23, 1600–1607.PubMedCrossRef Ortiz, A., Oliveira, J. P., Waldek, S., Warnock, D. G., Cianciaruso, B., Wanner, C., et al. (2008a). Nephropathy in males and females with Fabry disease: cross-sectional description of patients before treatment with enzyme replacement therapy. Nephrology, Dialysis, Transplantation, 23, 1600–1607.PubMedCrossRef
go back to reference Ortiz, A., Oliveira, J. P., Wanner, C., Brenner, B. M., Waldek, S., & Warnock, D. G. (2008b). Recommendations and guidelines for the diagnosis and treatment of Fabry nephropathy in adults. Nature Clinical Practice Nephrology, 4(6), 327–336.PubMedCrossRef Ortiz, A., Oliveira, J. P., Wanner, C., Brenner, B. M., Waldek, S., & Warnock, D. G. (2008b). Recommendations and guidelines for the diagnosis and treatment of Fabry nephropathy in adults. Nature Clinical Practice Nephrology, 4(6), 327–336.PubMedCrossRef
go back to reference Ramaswami, U., Whybra, C., Parini, R., et al. (2006). Clinical manifestations of Fabry disease in children: data from the Fabry Outcome Survey. Acta Paediatrica, 95, 86–92.PubMedCrossRef Ramaswami, U., Whybra, C., Parini, R., et al. (2006). Clinical manifestations of Fabry disease in children: data from the Fabry Outcome Survey. Acta Paediatrica, 95, 86–92.PubMedCrossRef
go back to reference Resta, R. G. (Ed.). (2000). Psyche and helix, Psychological aspects of genetic counseling. Essays by Seymour Kessler, PhD. New York: Wiley-Liss. Resta, R. G. (Ed.). (2000). Psyche and helix, Psychological aspects of genetic counseling. Essays by Seymour Kessler, PhD. New York: Wiley-Liss.
go back to reference Ries, M., Gupta, S., Moore, D. F., Sachdev, V., Quirk, J. M., Murray, G. J., et al. (2005). Pediatric Fabry disease. Pediatrics, 115(3), e344–e355. Resta RG (ed) (2000).PubMedCrossRef Ries, M., Gupta, S., Moore, D. F., Sachdev, V., Quirk, J. M., Murray, G. J., et al. (2005). Pediatric Fabry disease. Pediatrics, 115(3), e344–e355. Resta RG (ed) (2000).PubMedCrossRef
go back to reference Schiffmann, R., Murray, G. J., Treco, D., Daniel, P., Sellos-Moura, M., Myers, M., et al. (2000). Infusion of α-galactosidase A reduces tissue globotriaosylceramide storage in patients with Fabry disease. PNAS, 97, 365–370. Schiffmann, R., Murray, G. J., Treco, D., Daniel, P., Sellos-Moura, M., Myers, M., et al. (2000). Infusion of α-galactosidase A reduces tissue globotriaosylceramide storage in patients with Fabry disease. PNAS, 97, 365–370.
go back to reference Schiffmann, R., Kopp, J. B., Austin, H. A., Sabnis, S., Moore, D. F., Weibel, T., et al. (2001). Enzyme replacement therapy in Fabry disease. A randomized controlled trial. Journal of the American Medical Association, 285, 2743–2749.PubMedCrossRef Schiffmann, R., Kopp, J. B., Austin, H. A., Sabnis, S., Moore, D. F., Weibel, T., et al. (2001). Enzyme replacement therapy in Fabry disease. A randomized controlled trial. Journal of the American Medical Association, 285, 2743–2749.PubMedCrossRef
go back to reference Scott, C. R., Elliot, S., Glass, M., Buroker, N., Thomas, L., Keutzer, J., et al. (2011). Gelb MH (2011) Application of a triplex assay by MS/MS for the detection of Fabry, Pompe, and MPS-I within a newborn screening laboratory. 7th WORLD symposium Scott, C. R., Elliot, S., Glass, M., Buroker, N., Thomas, L., Keutzer, J., et al. (2011). Gelb MH (2011) Application of a triplex assay by MS/MS for the detection of Fabry, Pompe, and MPS-I within a newborn screening laboratory. 7th WORLD symposium
go back to reference Sims, K., Politei, J., Banikazemi, M., & Lee, P. (2009). Stroke in Fabry disease frequently occurs before diagnosis and in the absence of other clinical events: Natural history data from the Fabry registry. Stroke, 40, 788–794.PubMedCrossRef Sims, K., Politei, J., Banikazemi, M., & Lee, P. (2009). Stroke in Fabry disease frequently occurs before diagnosis and in the absence of other clinical events: Natural history data from the Fabry registry. Stroke, 40, 788–794.PubMedCrossRef
go back to reference Sørensen, S. A., & Hasholt, L. (1983). Attitudes of persons at risk for Fabry’s disease towards predictive tests and genetic counseling. Journal of Biosocial Science, 15, 89–94.PubMedCrossRef Sørensen, S. A., & Hasholt, L. (1983). Attitudes of persons at risk for Fabry’s disease towards predictive tests and genetic counseling. Journal of Biosocial Science, 15, 89–94.PubMedCrossRef
go back to reference Street, N. J., Yi, M. S., Bailey, L. A., & Hopkin, R. J. (2006). Comparison of health-related quality of life between heterozygous women with Fabry disease, a healthy control population, and patients with other chronic disease. Genetics in Medicine, 8(6), 346–353.PubMedCrossRef Street, N. J., Yi, M. S., Bailey, L. A., & Hopkin, R. J. (2006). Comparison of health-related quality of life between heterozygous women with Fabry disease, a healthy control population, and patients with other chronic disease. Genetics in Medicine, 8(6), 346–353.PubMedCrossRef
go back to reference Tøndel, C., Bostad, L., Larsen, K., et al. (2013). Agalsidase benefits renal hisotology in young patients with Fabry disease. Journal of the American Society of Nephrology, 24, 137–148.PubMedCrossRef Tøndel, C., Bostad, L., Larsen, K., et al. (2013). Agalsidase benefits renal hisotology in young patients with Fabry disease. Journal of the American Society of Nephrology, 24, 137–148.PubMedCrossRef
go back to reference Uhlmann, W. R., Schuette, J. L., & Yashar, B. (2009). A guide to genetic counseling (2nd ed.). Hoboken: Wiley Blackwell. Uhlmann, W. R., Schuette, J. L., & Yashar, B. (2009). A guide to genetic counseling (2nd ed.). Hoboken: Wiley Blackwell.
go back to reference Vedder, A. C., Linthorst, G. E., Houge, G., Groener, J. E., Ormel, E. E., Bouma, B. J., et al. (2007). Treatment of Fabry disease: outcome of a comparative trial with agalsidase alfa or beta at a dose of 0.2mg/kg. PLoS One, 2(7), e598.PubMedCrossRef Vedder, A. C., Linthorst, G. E., Houge, G., Groener, J. E., Ormel, E. E., Bouma, B. J., et al. (2007). Treatment of Fabry disease: outcome of a comparative trial with agalsidase alfa or beta at a dose of 0.2mg/kg. PLoS One, 2(7), e598.PubMedCrossRef
go back to reference Waldek, S., Patel, M. R., Banikazemi, M., Lemay, R., & Lee, P. (2009). Life expectancy and cause of death in males and females with Fabry disease: findings from the Fabry registry. Genetics in Medicine, 11(11), 790–796.PubMedCrossRef Waldek, S., Patel, M. R., Banikazemi, M., Lemay, R., & Lee, P. (2009). Life expectancy and cause of death in males and females with Fabry disease: findings from the Fabry registry. Genetics in Medicine, 11(11), 790–796.PubMedCrossRef
go back to reference Wang, R. Y., Lelis, A., Mirocha, J., & Wilcox, W. R. (2007). Heterozygous Fabry women are not just carriers, but have a significant burden of disease and impaired quality of life. Genetics in Medicine, 9(1), 34–45.PubMedCrossRef Wang, R. Y., Lelis, A., Mirocha, J., & Wilcox, W. R. (2007). Heterozygous Fabry women are not just carriers, but have a significant burden of disease and impaired quality of life. Genetics in Medicine, 9(1), 34–45.PubMedCrossRef
go back to reference Wang, R. Y., Bodamer, O. A., Watson, M. S., Wilcox, W. R., & on behalf of the ACMG Work Group on Diagnostic Confirmation of Lysosomal Storage Diseases. (2011). Lysosomal storage diseases: diagnostic confirmation and management of presymptomatic individuals. Genetics in Medicine, 13(5), 457–484.PubMedCrossRef Wang, R. Y., Bodamer, O. A., Watson, M. S., Wilcox, W. R., & on behalf of the ACMG Work Group on Diagnostic Confirmation of Lysosomal Storage Diseases. (2011). Lysosomal storage diseases: diagnostic confirmation and management of presymptomatic individuals. Genetics in Medicine, 13(5), 457–484.PubMedCrossRef
go back to reference Watt, T., Burlina, A. P., Cazzorla, C., Schönfeld, D., Banikazemi, M., Hopkin, R. J., et al. (2010). Agalsidase beta treatment is associated with improved quality of life in patients with Fabry disease: findings from the Fabry Registry. Genetics in Medicine, 12(11), 703–712.PubMedCrossRef Watt, T., Burlina, A. P., Cazzorla, C., Schönfeld, D., Banikazemi, M., Hopkin, R. J., et al. (2010). Agalsidase beta treatment is associated with improved quality of life in patients with Fabry disease: findings from the Fabry Registry. Genetics in Medicine, 12(11), 703–712.PubMedCrossRef
go back to reference Weil, J. (2000). Psychosocial genetic counseling. Oxford: Oxford University Press. Weil, J. (2000). Psychosocial genetic counseling. Oxford: Oxford University Press.
go back to reference Wertz, D., Fanos, J. H., & Reilly, P. R. (1994). Genetic testing for children and adolescents: who decides? Journal of the American Medical Association, 272, 875–881.PubMedCrossRef Wertz, D., Fanos, J. H., & Reilly, P. R. (1994). Genetic testing for children and adolescents: who decides? Journal of the American Medical Association, 272, 875–881.PubMedCrossRef
go back to reference Wilcox, W. R., Oliveira, J. P., Hopkin, R. J., Ortiz, A., Banikazemi, M., Feldt-Rasmussen, U., et al. (2008). Females with Fabry disease frequently have major organ involvement: lessons from the Fabry registry. Molecular Genetics and Metabolism, 93(2), 112–128.PubMedCrossRef Wilcox, W. R., Oliveira, J. P., Hopkin, R. J., Ortiz, A., Banikazemi, M., Feldt-Rasmussen, U., et al. (2008). Females with Fabry disease frequently have major organ involvement: lessons from the Fabry registry. Molecular Genetics and Metabolism, 93(2), 112–128.PubMedCrossRef
go back to reference Williams, J. K., Schutte, D. L., Evers, C., & Holkup, P. A. (2000). Redefinition: coping with normal results from predictive gene testing for neurodegenerative disorders. Research in Nursing & Health, 23, 260–269.CrossRef Williams, J. K., Schutte, D. L., Evers, C., & Holkup, P. A. (2000). Redefinition: coping with normal results from predictive gene testing for neurodegenerative disorders. Research in Nursing & Health, 23, 260–269.CrossRef
go back to reference Wise, D., Wallace, H. F., & Jellinek, E. H. (1962). Angiokeratoma corporis diffusum. Oxford Journals Medicine New Series, XXXI(122), 177–212. Wise, D., Wallace, H. F., & Jellinek, E. H. (1962). Angiokeratoma corporis diffusum. Oxford Journals Medicine New Series, XXXI(122), 177–212.
go back to reference Yasuda, M., Shabbeer, J., Benson, S. D., Maire, I., Burnett, R. M., & Desnick, R. J. (2003). Fabry disease: characterization of alpha-galactosidase A double mutations and the D313Y plasma enzyme pseudodeficiency allele. Human Mutation, 22, 486–492.PubMedCrossRef Yasuda, M., Shabbeer, J., Benson, S. D., Maire, I., Burnett, R. M., & Desnick, R. J. (2003). Fabry disease: characterization of alpha-galactosidase A double mutations and the D313Y plasma enzyme pseudodeficiency allele. Human Mutation, 22, 486–492.PubMedCrossRef
Metadata
Title
Fabry Disease Practice Guidelines: Recommendations of the National Society of Genetic Counselors
Authors
Dawn A. Laney
Robin L. Bennett
Virginia Clarke
Angela Fox
Robert J. Hopkin
Jack Johnson
Erin O’Rourke
Katherine Sims
Gerald Walter
Publication date
01-10-2013
Publisher
Springer US
Published in
Journal of Genetic Counseling / Issue 5/2013
Print ISSN: 1059-7700
Electronic ISSN: 1573-3599
DOI
https://doi.org/10.1007/s10897-013-9613-3

Other articles of this Issue 5/2013

Journal of Genetic Counseling 5/2013 Go to the issue