Nephropathic cystinosis

An autosomal recessive condition caused by mutation(s) in the CTNS gene, encoding cystinosin. It is a sub-type of cystinosis, in which accumulation of cystine in the kidney results in renal dysfunction.

Also known as: Abderhalden Kaufmann Lignac syndrome, Abderhalden Lignac Kaufmann disease, Abderhalden-Kaufmann-Lignac syndrome, Abderhalden-Lignac-Kaufmann disease, CTNS, cystinosis, atypical nephropathic, cystinosis, nephropathic

4 clinical trials for this condition and its sub-types.