NirvanamKnowledge · Cases · Solver

Congenital Disorder

Cystinosis

AMW:DIS:160128

A metabolic disease characterized by the defective transport of CYSTINE across the lysosomal membrane due to mutation of a membrane protein cystinosin. This results in cystine accumulation and crystallization in the cells causing widespread tissue damage. In the KIDNEY, nephropathic cystinosis is a common cause of RENAL FANCONI SYNDROME.

Pathology clinical

Graph assertions

Embed this node