Cystinosis
Summary
Cystinosis is a rare, progressive genetic disorder caused by a mutation in the CTNS gene, which results in the build-up of cystine amino acid in the body. CTNS gene encodes for cystinosin protein, which transports cystine protein out of lysosomes. When it malfunctions, that's when the amino acid accumulates and causes cystinosis. Symptoms include blindness, kidney failure, and muscle weakness.
Sources
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- "Cystinosis" New England Journal of Medicine (2002)
- "The de Toni-Fanconi Syndrome with Cystinosis" A.M.A. Journal of Diseases of Children (1958)
- "Lysosomal cystine accumulation promotes mitochondrial depolarization and induction of redox-sensitive genes in human kidney proximal tubular cells" The Journal of Physiology (2016)