نتایج جستجو برای: ژن cyp21a2

تعداد نتایج: 16028  

2017
Sudhisha Dubey Veronique Tardy Madhumita Roy Chowdhury Neerja Gupta Vandana Jain Deepika Deka Pankaj Sharma Yves Morel Madhulika Kabra

BACKGROUND & OBJECTIVES Congenital adrenal hyperplasia (CAH) is an autosomal recessive disorder with a wide range of clinical manifestations. The disease is attributed to mutations in CYP21A2 gene encoding 21-hydroxylase enzyme. In view of severe phenotype in salt-losing cases, issues related to genital ambiguity in girls and precocity in boys, most families opt for prenatal testing and termina...

2014
Francis K. Yoshimoto Hwei-Ming Peng Haoming Zhang Sean M. Anderson Richard J. Auchus

Some cytochrome P450 enzymes epoxidize unsaturated substrates, but this activity has not been described for the steroid hydroxylases. Physiologic steroid substrates, however, lack carbon-carbon double bonds in the parts of the pregnane molecules where steroidogenic hydroxylations occur. Limited data on the reactivity of steroidogenic P450s toward olefinic substrates exist, and the study of occu...

2011
Jan Idkowiak Stephen O'Riordan Nicole Reisch Ewa M. Malunowicz Felicity Collins Michiel N. Kerstens Birgit Köhler Luitgard Margarete Graul-Neumann Maria Szarras-Czapnik Mehul Dattani Martin Silink Cedric H. L. Shackleton Dominique Maiter Nils Krone Wiebke Arlt

CONTEXT P450 oxidoreductase (POR) is a crucial electron donor to all microsomal P450 cytochrome (CYP) enzymes including 17α-hydroxylase (CYP17A1), 21-hydroxylase (CYP21A2) and P450 aromatase. Mutant POR causes congenital adrenal hyperplasia with combined glucocorticoid and sex steroid deficiency. P450 oxidoreductase deficiency (ORD) commonly presents neonatally, with disordered sex development ...

2014
Melisa Taboas Luciana Gómez Acuña María Florencia Scaia Carlos D. Bruque Noemí Buzzalino Mirta Stivel Nora R. Ceballos Liliana Dain

Congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency is the most frequent inborn error of metabolism and accounts for 90-95% of CAH cases. In the present work, we analyzed the functional consequence of four novel previously reported point CYP21A2 mutations -p.R132C, p.R149C, p.M283V, p.E431K- found in Argentinean 21-hydroxylase deficient patients. In addition, we report an acce...

2015
Roseane Lopes da Silva-Grecco Débora de Paula Michelatto Carolina Rodrigues Lincoln-de-Carvalho Pamela Pontes Henrique Heloísa Marcelina da Cunha Maricilda Palandi-de-Mello

Congenital adrenal hyperplasia, one of the most frequent autosome recessive disorders, is caused by defects in steroidogenic enzymes involved in the cortisol biosynthesis. Approximately 95% of the cases are caused by abnormal function of the 21-hydroxylase enzyme. This deficiency leads to androgen excess, consequently, to virilization and rapid somatic growth with accelerated skeletal maturatio...

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