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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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| Publicado en: | Ann Med Health Sci Res |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Medknow Publications & Media Pvt Ltd
2016
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4924496/ https://ncbi.nlm.nih.gov/pubmed/27398254 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/2141-9248.183935 |
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