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Up to: Inborn carbohydrate metabolic disorder · Classic organic aciduria · Inborn error of biotin metabolism
Multiple carboxylase deficiency
Multiple carboxylase deficiency (MCD) is a term used to describe inborn errors of biotin metabolism characterized by reduced activities of biotin-dependent enzymes resulting in a wide spectrum of symptoms, including feeding difficulty, breathing difficulties, lethargy, seizures, skin rash, alopecia, and developmental delay.
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Biotinidase deficiency 3 trials