نتایج جستجو برای: biotinidase deficiency

تعداد نتایج: 137210  

Journal: :Nutrition reviews 2006
Yousef I Hassan Janos Zempleni

Covalent modifications of histones are a crucial component of epigenetic events that regulate chromatin structures and gene function. Evidence exists that distinct lysine residues in histones are modified by covalent attachment of the vitamin biotin, catalyzed by biotinidase and holocarboxylase synthetase. Biotinylation of histones appears to be conserved across species. The following biotinyla...

Journal: :Brain & development 2009
Mutluay Arslan Sebahattin Vurucu Necati Balamtekin Bulent Unay Ridvan Akin Ismail Kurt Okan Ozcan

Valproic acid (VPA) is a widely used and well-tolerable antiepileptic drug in epileptic patients. However, VPA has many side effects dose-dependent or non-dose-dependent. It is reported that VPA treatment may lead to biotin deficiency and low serum and liver tissue biotinidase enzyme activity (BEA). Major clinical manifestations in biotin deficiency are seborrheic dermatitis, dry skin, fine and...

Journal: :Human mutation 2008
Lisa M Bailey Ruby A Ivanov Sarawut Jitrapakdee Callum J Wilson John C Wallace Steven W Polyak

Multiple carboxylase deficiency is a clinical condition caused by defects in the enzymes involved in biotin metabolism, holocarboxylase synthetase (HLCS) or biotinidase. HLCS deficiency is a potentially fatal condition if left untreated, although the majority of patients respond to oral supplementation of 10-20 mg/day of biotin. Patients who display incomplete responsiveness to this therapy hav...

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