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Mutation analysis of androgen receptor gene: multiple uses for a single test.

Abstract
Androgen receptor gene mutations are one of the leading causes of disorders of sex development (DSD) exhibited by sexual ambiguity or sex reversal. In this study, 2 families with patients whom diagnosed clinically as androgen insensitivity syndrome (AIS) were physically and genetically examined. This evaluation carried out by cytogenetic and molecular analysis including karyotype and sequencing of SRY and AR genes. In family 1, two brothers and their mother were hemizygous and heterozygous respectively for c.2522G>A variant, while one of their healthy brother was a completely normal hemizygote. Family 2 assessment demonstrated the c.639G>A (rs6152) mutation in two siblings who were reared as girls. The SRY gene was intact in all of the study's participants. Our findings in family 1 could be a further proof for the pathogenicity of the c.2522G>A variant. Given the importance of AR mutations in development of problems such as sex assignment in AIS patients, definitive diagnosis and phenotype-genotype correlation could be achieved by molecular genetic tests that in turn could have promising impacts in clinical management and also in prenatal diagnosis of prospect offspring. In this regard, phenotype-genotype correlation could be helpful and achieved by molecular genetic tests. This could influence the clinical management of the patients as well as prenatal diagnosis for the prospective offspring.
AuthorsAzadeh Shojaei, Farkhondeh Behjati, Reza Ebrahimzadeh-Vesal, Maryam Razzaghy-Azar, Pupak Derakhshandeh-Peykar, Pantea Izadi, Abdol-Mohammad Kajbafzadeh, Mohammad-Ali Dowlatih, Fatemeh Karami, Javad Tavakkoly-Bazzaz
JournalGene (Gene) Vol. 552 Issue 2 Pg. 234-8 (Dec 01 2014) ISSN: 1879-0038 [Electronic] Netherlands
PMID25241384 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
CopyrightCopyright © 2014 Elsevier B.V. All rights reserved.
Chemical References
  • Receptors, Androgen
Topics
  • Androgen-Insensitivity Syndrome (diagnosis, genetics, pathology, psychology)
  • DNA Mutational Analysis
  • Female
  • Humans
  • Male
  • Pedigree
  • Point Mutation
  • Receptors, Androgen (genetics)

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