Variants
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Isovaleryl-CoA dehydrogenase deficiency

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Description

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).

OMIM

  • Mode of Inheritance

  • Autosomal recessive inheritance

VARIANTS

206

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Genes

External Links

  • OMIM

    243500

  • Orphanet

    33

  • HPO
  • Medgen

    C0268575

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