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.

Also known as: MCD, multiple carboxylase deficiency

4 clinical trials for this condition and its sub-types, 0 tagged with Multiple carboxylase deficiency itself.