Propionic acidemia

An organic aciduria caused by the deficient activity of the propionyl Coenzyme A carboxylase and is characterized by life threatening episodes of metabolic decompensation, neurological dysfunction and that may be complicated by cardiomyopathy.

Also known as: GLYCINEMIA, ketotic, ketotic hyperglycinemia, propionic acidemia, propionic aciduria, propionyl-CoA carboxylase deficiency, Propionicacidemia, prop

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