What does Biotinidase deficiency mean?
Definitions for Biotinidase deficiency
bi·o·tinidase de·fi·cien·cy
This dictionary definitions page includes all the possible meanings, example usage and translations of the word Biotinidase deficiency.
Wikidata
Biotinidase deficiency
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. This situation results in biotin deficiency. Biotin, sometimes called vitamin B7, is an important water-soluble nutrient that aids in the metabolism of fats, carbohydrates and proteins. Biotin deficiency can result in behavioral disorders, lack of coordination, learning disabilities and seizure. Biotin supplementation can alleviate and sometimes totally arrest such symptoms.
U.S. National Library of Medicine
Biotinidase Deficiency
The late onset form of MULTIPLE CARBOXYLASE DEFICIENCY (deficiency of the activities of biotin-dependent enzymes propionyl-CoA carboxylase, methylcrotonyl-CoA carboxylase, and PYRUVATE CARBOXYLASE) due to a defect or deficiency in biotinidase which is essential for recycling BIOTIN.
Numerology
Chaldean Numerology
The numerical value of Biotinidase deficiency in Chaldean Numerology is: 7
Pythagorean Numerology
The numerical value of Biotinidase deficiency in Pythagorean Numerology is: 1
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"Biotinidase deficiency." Definitions.net. STANDS4 LLC, 2024. Web. 25 Apr. 2024. <https://www.definitions.net/definition/Biotinidase+deficiency>.
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