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Fabry's Disease: Case Series and Review of Literature

Fabry's disease is an X-linked lysosomal storage disorder caused by a deficiency of alpha-galactosidase A enzyme with the progressive accumulation of globotriaosylceramide in vascular endothelial cells leading to cardiovascular, renal, gastrointestinal, neuropathic, lenticular, and dermatologic...

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Detalles Bibliográficos
Autores principales:	Wani, Muzaffar Maqsood, Khan, Imran, Bhat, Riyaz Ahmad, Ahmad, Muzaffar
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Medknow Publications & Media Pvt Ltd 2016
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4924496/ https://www.ncbi.nlm.nih.gov/pubmed/27398254 http://dx.doi.org/10.4103/2141-9248.183935

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