Inborn branched chain aminoaciduria (medical condition)

Any inherited disorder that results in abnormally high levels of branched chain amino acids in the urine. Branched chain amino acids includes leucine, valine and isoleucine. Maple syrup urine disease is the main inborn disorder that causes this form of aminoaciduria. See also Inborn branched chain aminoaciduria

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.