Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/109153
Type: Artigo de periódico
Title: Molecular Diagnosis Of 5α-reductase Type Ii Deficiency In Brazilian Siblings With 46,xy Disorder Of Sex Development
Author: de Calais F.L.
Soardi F.C.
Petroli R.J.
Lusa A.L.G.
de Paiva e Silva R.B.
Maciel-Guerra A.T.
Guerra-Junior G.
de Mello M.P.
Abstract: The steroid 5α-reductase type II enzyme catalyzes the conversion of testosterone (T) to dihydrotestosterone (DHT), and its deficiency leads to undervirilization in 46,XY individuals, due to an impairment of this conversion in genital tissues. Molecular analysis in the steroid 5α-reductase type II gene (SRD5A2) was performed in two 46,XY female siblings. SRD5A2 gene sequencing revealed that the patients were homozygous for p.Gln126Arg missense mutation, which results from the CGA > CAA nucleotide substitution. The molecular result confirmed clinical diagnosis of 46,XY disorder of sex development (DSD) for the older sister and directed the investigation to other family members. Studies on SRD5A2 protein structure showed severe changes at NADPH binding region indicating that structural modeling analysis can be useful to evaluate the deleterious role of a mutation as causing 5α-reductase type II enzyme deficiency. © 2011 by the authors; licensee MDPI, Basel, Switzerland.
Editor: 
Rights: aberto
Identifier DOI: 10.3390/ijms12129471
Address: http://www.scopus.com/inward/record.url?eid=2-s2.0-84055200097&partnerID=40&md5=57917ad979ed5e56415949397a8e58e4
Date Issue: 2011
Appears in Collections:Unicamp - Artigos e Outros Documentos

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