tailieunhanh - Cornea Verticillata in classical Fabry disease, first from Sri Lanka: A case report

Fabry disease is a rare inborn error of metabolism with profound clinical consequences if untreated. It is caused by the deficiency of α galactosidase A enzyme and is the only lysosomal storage disorder with an X linked inheritance. | Cornea Verticillata in classical Fabry disease first from Sri Lanka A case report

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