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Up to: Classic organic aciduria · Inborn disorder of branched-chain amino acid metabolism · Valine metabolism disease
3-hydroxyisobutyric aciduria
3 hydroxyisobutyric aciduria is characterized by ketoacidotic episodes, cerebral anomalies and facial dysmorphism. It is an organic aciduria that involves valine metabolism. Thirteen cases have been described in the literature so far. Transmission is thought to be autosomal recessive.
This condition has no sub-types.