Female with Fabry Disease Unknowingly Donates Affected Kidney to Sister: A Call for Pre-transplant Genetic Testing
Author:
Publisher
Springer Berlin Heidelberg
Link
http://link.springer.com/content/pdf/10.1007/8904_2011_108
Reference20 articles.
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2. Bloomfield SE, David DS, Rubin AL (1978) Eye findings in the diagnosis of Fabry’s disease. Patients with renal failure. JAMA 240:647–649
3. Eng CM, Guffon N, Wilcox WR et al (2001) Safety and efficacy of recombinant human alpha-galactosidase A–replacement therapy in Fabry’s disease. N Engl J Med 345:9–16
4. Groth CG, Ringden O (1984) Transplantation in relation to the treatment of inherited disease. Transplantation 38:319–327
5. Kasiske BL, Ravenscraft M, Ramos EL, Gaston RS, Bia MJ, Danovitch GM (1996) The evaluation of living renal transplant donors: clinical practice guidelines. Ad Hoc Clinical Practice Guidelines Subcommittee of the Patient Care and Education Committee of the American Society of Transplant Physicians. J Am Soc Nephrol 7:2288–2313
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4. A case of latent heterozygous Fabry disease in a female living kidney donor candidate;CEN Case Reports;2020-07-25
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