A Single Lung Transplant in a Patient with Fabry Disease: Causality or Far-Fetched? A Case Report

Introduction. Fabry disease is a rare X-linked lysosomal storage disorder, characterized by an α-galactosidase A deficiency resulting in globotriaosylceramide storage within cells. Subsequently, various organ systems are involved, clinically the most important are kidneys, the heart, and the periphe...

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Detalles Bibliográficos
Autores principales: Gaggl, Martina, Kain, Renate, Jaksch, Peter, Haider, Dominik, Mundigler, Gerald, Voigtländer, Till, Sunder-Plassmann, Raute, Rommer, Paulus, Klepetko, Walter, Sunder-Plassmann, Gere
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3638525/
https://www.ncbi.nlm.nih.gov/pubmed/23691425
http://dx.doi.org/10.1155/2013/905743

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3638525/
https://www.ncbi.nlm.nih.gov/pubmed/23691425
http://dx.doi.org/10.1155/2013/905743

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