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  • Biotinidase - Wikipedia
    Biotinidase (EC 3 5 1 12, amidohydrolase biotinidase, BTD), also known as biotinase, [1] is an enzyme that in humans is encoded by the BTD gene The enzyme breaks down biotin amides, releasing free biotin and the amine
  • Biotinidase Deficiency - Symptoms, Causes, Treatment | NORD
    Learn about Biotinidase Deficiency, including symptoms, causes, and treatments If you or a loved one is affected by this condition, visit NORD to find
  • Biotinidase Deficiency - GeneReviews® - NCBI Bookshelf
    Symptoms of untreated profound biotinidase deficiency (<10% mean normal serum biotinidase activity) usually appear between ages one week and ten years, typically with optic atrophy, hypotonia, seizures, hair loss, and skin rash Affected children often have ataxia and developmental delay
  • Biotinidase deficiency: MedlinePlus Genetics
    Biotinidase deficiency is an inherited disorder in which the body is unable to recycle the vitamin biotin If this condition is not recognized and treated, its signs and symptoms typically appear within the first few months of life, although it can also become apparent later in childhood
  • Biotinidase deficiency | About the Disease | GARD
    Biotinidase deficiency is an inherited disorder in which the body is unable to recycle the vitamin biotin
  • Biotin and biotinidase deficiency - PMC
    Biotin-dependent carboxylases catalyze the fixation of bicarbonate in organic acids and play crucial roles in the metabolism of fatty acids, amino acids and glucose Carboxylase activities decrease substantially in response to biotin deficiency
  • Biotinidase Deficiency: Causes Symptoms - Medicover Hospitals
    Biotinidase deficiency is an inherited metabolic disorder characterized by the body's inability to release free biotin from proteins in the diet Biotin, also known as vitamin B7, is essential for various metabolic processes, including the synthesis of fatty acids, amino acids, and glucose
  • Biotinidase deficiency - Wikipedia
    Biotinidase deficiency is an autosomal recessive metabolic disorder in which biotin is not released from proteins in the diet during digestion or from normal protein turnover in the cell




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