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Biotinidase Deficiency in Newborns as Respiratory Distress and Tachypnea: A Case Report
OBJECTIVE: Biotin is a coenzyme composed of four carboxylases. It presents in amino acid catabolism, fatty acid synthesis, and gluconeogenesis. Biotinidase recycles the vitamin biotin. A biotinidase deficiency is a neurocutaneous disorder with autosomal recessive inheritance. The symptoms can be suc...
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| Vydáno v: | Iran J Child Neurol |
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| Hlavní autoři: | , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Shahid Beheshti University of Medical Sciences
2015
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4515343/ https://ncbi.nlm.nih.gov/pubmed/26221165 |
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