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Diseases

Genetic and Rare Diseases Information Center (GARD)

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Isobutyryl-CoA dehydrogenase deficiency

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Other Names for this Disease

  • ACAD8 deficiency
  • Acyl-CoaA dehydrogenase family, member 8, deficiency of
  • IBD deficiency
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Your Questions Answered


1 question(s) from the public on this disease have been answered. Submit a new question.
  • My son was diagnosed with isobutyryl-CoA dehydrogenase deficiency (IBD deficiency) at birth. He is 7 months old and very healthy with no signs or symptoms. He is being followed by a specialist, gets regular blood tests, and follows a special diet. Will this condition be with him for the rest of his life? Is there anything that we can do for him? Click here for answer

Other Names for this Disease
  • ACAD8 deficiency
  • Acyl-CoaA dehydrogenase family, member 8, deficiency of
  • IBD deficiency
See Disclaimer regarding information on this site. Some links on this page may take you to organizations outside of the National Institutes of Health.