multiple carboxylase deficiencies การใช้

• This disorder is classified as a multiple carboxylase deficiency, a group of disorders characterized by impaired activity of certain enzymes that depend on biotin.
• These include 4-Hydroxybutyric aciduria, 3-methylglutaconyl-Co A hydratase deficiency, multiple carboxylase deficiency, methylmalonic acidemia, and propionic acidemia.
• :In some inborn errors of metabolism there can be a distinctive body odor ( examples : " mouse-like " odor in phenylketonuria, " maple syrup " odor in maple syrup urine disease, " sweaty feet " odor in isovaleric acidemia, " male cat urine " odor in multiple carboxylase deficiency, " cabbage " or " rancid butter " odor in type I tyrosinemia ).