biocytinase

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biocytinase

[‚bī·ō′sīt·ən‚ās]
(biochemistry)
An enzyme present in the blood and liver which hydrolyzes biocytin into biotin and lysine.
References in periodicals archive ?
Light-colored hair can be seen in phenylketonuria and trichorhexis nodosa; pili torti can be seen in ectodermal dysplasia, argininosuccinic aciduria, or biotinidase deficiency.
But it has now been revealed Taylor has Biotinidase deficiency, a genetic condition which mimics the affects of mitochondrial disease.
822, de 6 de junho de 2001) com o intuito de realizar, gratuitamente, os exames para diagnostico de doencas congenitas, tais como: Fenilcetonuria, Hipotireoidismo Congenito, Doenca Falciforme, Fibrose Cistica, Deficiencia de Biotinidase e Hiperplasia Adrenal Congenita.
Amir, "Reversible deafness caused by biotinidase deficiency," Pediatric Neurology, vol.
In our country, phenylketonuria, congenital hypothyroidism, biotinidase deficiency, and cystic fibrosis are included in the neonatal screening program, but galactosemia has not yet been included in this scope.
It affects all major aetiological factors involved in the pathogenesis of acne vulgaris (AV).1 In addition to a variety of clinical side- effects, Iso may cause dyslipidaemia, increased liver enzymes, and reduction of biotinidase activity.2 There are studies indicating elevation in homocysteine(Hcy) levels after treatment with Iso.3-6
Receiving about 300 newborns per month, the outpatient unit performs newborn metabolic screening (Guthrie test or heel pick test), which can be standard, conducting examinations such as TSH, T4, and phenylketonuria and cystic fibrosis; or extended, including examinations such as: G.6PD Deficiency, aminoacidopathies, congenital toxoplasmosis, biotinidase deficiency, galactosemia, and 17OH.
Anytime you turn the skin over consistently, you often need a lot of zinc." Mimickers of zinc deficiency include biotinidase deficiency, methylmalonic acidemia, propionic acidemia, maple syrup urine disease, citrullinemia, and ornithine transcarbamylase deficiency.
Bushra Afroze Clinical Geneticist from Aga Khan University was the next speaker and she talked about Biotinidase deficiency- Clinical Presentation, Diagnosis and Treatment.
VACTERL association: a new case with biotinidase deficiency and annular pancreas.
Metabolic and nutritional disorders like multiple carboxylase (holocarboxylase synthetase and biotinidase), essential fatty and amino acid deficiency may be life threatening.