Literature DB >> 18097518

Molecular diagnosis of 5alpha-reductase-2 gene mutation in two Indian families with male pseudohermaphroditism.

Marumudi Eunice1, Pascal Philibert, Bindu Kulshreshtha, Francoise Audran, Francoise Paris, Madan L Khurana, Praveen E Pulikkanath, Kiran Kucheria, Charles Sultan, Ariachery C Ammini.   

Abstract

AIM: To identify the genotype of two Indians with male pseudohermaphroditism.
METHODS: Standard radioimmunoassay procedure was used for estimating hormonal levels. Conventional cytogenetic analysis was carried out for diagnosing the genetic sex in these subjects with genital ambiguity. Molecular analysis was carried out by standard polymerase chain reaction procedure using different sets of primers and reaction conditions specific for the 5alpha-reductase type 2 gene (SRD5A2) gene. Direct sequencing was carried out using the ABI Prism dye terminator sequencing kit and the ABI 310 sequencing apparatus.
RESULTS: We found an SRD5A2 gene mutation in exon 5, where arginine is substituted with glutamine (R246Q), in two males with pseudohermaphroditism and ambiguous genitalia from unrelated families. This is the first time this mutation has been reported in individuals from India.
CONCLUSION: Identification of the R246Q mutation of the SRD5A2 gene from two unrelated Indian families possibly extends the founder gene effect. (c) 2008, Asian Journal of Andrology, SIMM and SJTU. All rights reserved.

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Year:  2007        PMID: 18097518     DOI: 10.1111/j.1745-7262.2008.00350.x

Source DB:  PubMed          Journal:  Asian J Androl        ISSN: 1008-682X            Impact factor:   3.285


  5 in total

1.  5 α-reductase type 2 deficiency - response to dihydrotestosterone gel: correspondence.

Authors:  Iram Shabir; Eunice Marumudi; Ram Kumar; Angela Ann Joseph; Madan L Khurana; Manju Mehta; T Satish Chandra; Ariachery C Ammini
Journal:  Indian J Pediatr       Date:  2013-09-20       Impact factor: 1.967

2.  Molecular genetics and phenotype/genotype correlation of 5-α reductase deficiency in a highly consanguineous population.

Authors:  Meshael M Alswailem; Ohoud S Alzahrani; Lamyaa Alghofaili; Ebtesam Qasem; Mai Almohanaa; Afaf Alsagheir; Bassam Bin Abbas; Najya A Attia; Adnan Al Shaikh; Ali S Alzahrani
Journal:  Endocrine       Date:  2018-09-29       Impact factor: 3.633

3.  Novel mutation of SRD5A2 gene in a patient with 5α-reductase 2 deficiency from India.

Authors:  Iram Shabir; Eunice Marumudi; Madan L Khurana; Rajesh Khadgawat
Journal:  BMJ Case Rep       Date:  2012-10-30

4.  Phenotype, Sex of Rearing, Gender Re-Assignment, and Response to Medical Treatment in Extended Family Members with a Novel Mutation in the SRD5A2 Gene.

Authors:  Asma Deeb; Hana Al Suwaidi; Fakunle Ibukunoluwa; Salima Attia
Journal:  J Clin Res Pediatr Endocrinol       Date:  2016-04-18

5.  Genetic Analysis of 25 Patients with 5α-Reductase Deficiency in Chinese Population.

Authors:  Bing Han; Tong Cheng; Hui Zhu; Jie Yu; Wen-Jiao Zhu; Huai-Dong Song; Haijun Yao; Jie Qiao
Journal:  Biomed Res Int       Date:  2020-06-09       Impact factor: 3.411

  5 in total

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