Isovaleryl-CoA dehydrogenase deficiency
Your Results
Sign InDescription
Isovaleric acidemia is an inborn error of leucine metabolism caused by a deficiency of isovaleryl-CoA dehydrogenase. It can present with severe neonatal ketoacidosis leading to death, but in milder cases recurrent episodes of ketoacidosis of varying degree occur later in infancy and childhood (summary by Vockley et al., 1991).
Mode of Inheritance
- Autosomal recessive inheritance
VARIANTS
206