Literature DB >> 21962961

Identification of a novel mutation in exon 1 of androgen receptor gene in an azoospermic patient with mild androgen insensitivity syndrome: case report and literature review.

Umberto Goglia1, Cinzia Vinanzi, Daniela Zuccarello, Davide Malpassi, Pietro Ameri, Massimo Casu, Francesco Minuto, Carlo Foresta, Diego Ferone.   

Abstract

OBJECTIVE: To report a case of an azoospermic subject with mild androgen insensitivity syndrome (MAIS) and review the relevant literature.
DESIGN: Case report.
SETTING: Academic research hospital. PATIENT(S): A 49-year-old man with undermasculinized features and a history of cryptorchidism and azoospermia. INTERVENTION(S): Hormonal evaluation and genetic testing of the androgen receptor gene (AR). MAIN OUTCOME MEASURE(S): Hormonal levels and sequence chromatogram of the proband and his mother. RESULT(S): We found total T in the normal range and high levels of gonadotropins. Karyotype was 46,XY. Genetic testing identified a novel mutation of exon 1 of AR, which resulted in an alanine to serine substitution in the transactivation domain at codon 240 (A240S). Fourteen other mutations of exon 1 of AR have been associated with MAIS to date. CONCLUSION(S): The novel mutation A240S of AR is involved in MAIS, a syndrome associated with azoospermia.
Copyright © 2011 American Society for Reproductive Medicine. Published by Elsevier Inc. All rights reserved.

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Year:  2011        PMID: 21962961     DOI: 10.1016/j.fertnstert.2011.08.033

Source DB:  PubMed          Journal:  Fertil Steril        ISSN: 0015-0282            Impact factor:   7.329


  7 in total

1.  Androgen receptor exon 1 mutation causes androgen insensitivity by creating phosphorylation site and inhibiting melanoma antigen-A11 activation of NH2- and carboxyl-terminal interaction-dependent transactivation.

Authors:  William H Lagarde; Amanda J Blackwelder; John T Minges; Andrew T Hnat; Frank S French; Elizabeth M Wilson
Journal:  J Biol Chem       Date:  2012-02-13       Impact factor: 5.157

Review 2.  Experimental methods to preserve male fertility and treat male factor infertility.

Authors:  Kathrin Gassei; Kyle E Orwig
Journal:  Fertil Steril       Date:  2015-12-30       Impact factor: 7.329

3.  An infertile man with gynecomastia caused by a novel mutation of the androgen receptor gene.

Authors:  Hui-Ying Xu; Cheng-Di Li; Li-Li Tang; Ling-Ling Wang; Xia Yu; Xue-Mei Gu; Xiang-Yang Lin; Bi-Cheng Chen
Journal:  Asian J Androl       Date:  2015 May-Jun       Impact factor: 3.285

4.  An insertion mutation in the androgen receptor gene in a patient with azoospermia.

Authors:  Yun-Hao Chen; Hui-Ying Xu; Zhang-Yang Wang; Zhe-Hui Zhu; Cheng-Di Li; Zhi-Gang Wu; Bi-Cheng Chen
Journal:  Asian J Androl       Date:  2015 Sep-Oct       Impact factor: 3.285

5.  The consequences of mutations in the reproductive endocrine system.

Authors:  Donchan Choi
Journal:  Dev Reprod       Date:  2012-12

6.  A Novel Mutation in Human Androgen Receptor Gene Causing Partial Androgen Insensitivity Syndrome in a Patient Presenting with Gynecomastia at Puberty.

Authors:  Cemil Koçyiğit; Serdar Sarıtaş; Gönül Çatlı; Hüseyin Onay; Bumin Nuri Dündar
Journal:  J Clin Res Pediatr Endocrinol       Date:  2016-04-18

7.  Protein Arginine Methyltransferase 6 Involved in Germ Cell Viability during Spermatogenesis and Down-Regulated by the Androgen Receptor.

Authors:  Manling Luo; Yuchi Li; Huan Guo; Shouren Lin; Jianbo Chen; Qian Ma; Yanli Gu; Zhimao Jiang; Yaoting Gui
Journal:  Int J Mol Sci       Date:  2015-12-10       Impact factor: 5.923

  7 in total

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