Adult Refsum disease

A very rare, clinically variable, multisystemic metabolic disease, characterized by anosmia, early-onset retinitis pigmentosa and possible neurological manifestations, including neuropathy, and cerebellar ataxia, deafness, ichthyosis, skeletal abnormalities, and cardiac arrhythmia. It is characterized biochemically by accumulation of phytanic acid in plasma and tissues.

Also known as: HMSN 4, HMSN type IV, HSMN IV, Refsum Disease, Refsum disease, Refsum disease, adult, 1, Refsum disease, classic, Refsum's disease

5 clinical trials for this condition and its sub-types, 4 tagged with Adult Refsum disease itself.