- Biotinidase - Wikipedia
This enzyme allows the body to use and recycle the B vitamin biotin, sometimes called vitamin H Biotinidase extracts biotin from food because the body needs biotin in its free, unattached form
- 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 | Newborn Screening
Find information about newborn screening for Biotinidase deficiency, including causes, signs, symptoms, and treatment
- 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, Serum - Mayo Clinic Laboratories | Neurology Catalog
Biotinidase deficiency is an autosomal recessive disorder caused by variants in the biotinidase gene (BTD) Age of onset and clinical phenotype vary among individuals depending on the amount of residual biotinidase activity
- Biotinidase Deficiency - StatPearls - NCBI Bookshelf
Biotinidase is an enzyme present abundantly in the serum, kidneys, and liver Biotinidase deficiency can be partial (10 to 30% of enzyme activity) or profound (less than 30% of enzyme activity), significantly impacting the treatment approach Partial cases can have little or no symptoms
- 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
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