Alpha-methylacyl-CoA racemase deficiency (medical condition)

An inherited disorder characterized by an enzyme (Alpha-methyl-acyl-CoA racemase) deficiency, liver disease, epilepsy, polyneuropathy and eye problems. The neuropathy tends to start during adulthood. See also Liver disease - retinitis pigmentosa - polyneuropathy - epilepsy

Chemwatch
Privacy Overview

This website uses cookies so that we can provide you with the best user experience possible. Cookie information is stored in your browser and performs functions such as recognising you when you return to our website and helping our team to understand which sections of the website you find most interesting and useful.