3-Hydroxy-3-methylglutaryl-CoA lyase deficiency
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3-Hydroxy-3-methylglutaryl-CoA lyase deficiency is an uncommon inherited disorder in which the body cannot properly process the amino acid leucine.[1] Additionally, the disorder prevents the body from making ketones, which are used for energy during fasting.[citation needed]
Quick Facts Other names, Specialty ...
3-Hydroxy-3-methylglutaryl-CoA lyase deficiency | |
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Other names | HMG-CoA lyase deficiency or Hydroxymethylglutaric aciduria |
HMG-CoA | |
Specialty | Pediatrics |
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