Biotinidase Deficiency: Causes, Symptoms & Treatment
Biotinidase deficiency is a very rare inherited metabolic disorder. It occurs due to a genetic defect in the enzyme biotinidase. About one in 80,000 children is born with such an enzyme disorder. Newborn screening helps to make the diagnosis. What is biotinidase deficiency? Biotinidase deficiency, or BTD for short, belongs to the group of rare … Biotinidase Deficiency: Causes, Symptoms & Treatment