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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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Detaylı Bibliyografya
Yayımlandı:Iran J Child Neurol
Asıl Yazarlar: KOOHMANAEE, Shahin, ZARKESH, Marjaneh, TABRIZI, Manijeh, HASSANZADEH RAD, Afagh, DIVSHALI, Siamak, DALILI, Setila
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Shahid Beheshti University of Medical Sciences 2015
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC4515343/
https://ncbi.nlm.nih.gov/pubmed/26221165
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