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A Case of Fabry's Disease with Congenital Agammaglobulinemia

Fabry's disease is an X-linked lysosomal storage disorder caused by abnormalities in the α-galactosidase A (GLA) gene, which leads to a GLA deficiency and to the intracellular deposition of globotriaosylceramide (Gb3) within vascular endothelium and other tissues. It manifests as progressive mu...

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Detalles Bibliográficos
Autores principales:	Lee, Ki-Yeol, Jeon, Su-Young, Hong, Jin-Woo, Kim, Sung-Eun, Song, Ki-Hoon, Kim, Young-Hun, Kim, Ki-Ho
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	The Korean Academy of Medical Sciences 2011
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3124732/ https://www.ncbi.nlm.nih.gov/pubmed/21738355 http://dx.doi.org/10.3346/jkms.2011.26.7.966

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