Literature DB >> 9341880

Two SRY-negative XX male brothers without genital ambiguity.

J C Zenteno1, M López, C Vera, J P Méndez, S Kofman-Alfaro.   

Abstract

We report a Mexican family in which two sibs were identified as "classic" XX males without genital ambiguities. Molecular studies revealed that both patients were negative for several Y sequences, including SRY. A review of familial cases disclosed that this is the first family where a complete male phenotype was observed in Y-negative XX male non-twin brothers. These data suggest that an inherited loss-of-function mutation, in a gene participating in the sex-determining cascade, can induce normal male sexual differentiation in the absence of SRY.

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Year:  1997        PMID: 9341880     DOI: 10.1007/s004390050561

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  10 in total

Review 1.  Genetic disorders and male infertility.

Authors:  Shinnosuke Kuroda; Kimitsugu Usui; Hiroyuki Sanjo; Teppei Takeshima; Takashi Kawahara; Hiroji Uemura; Yasushi Yumura
Journal:  Reprod Med Biol       Date:  2020-06-27

2.  Clinical, cytogenetic, and molecular analysis with 46,XX male sex reversal syndrome: case reports.

Authors:  Xuefeng Gao; Guian Chen; Jing Huang; Quan Bai; Nan Zhao; Minjie Shao; Liping Jiao; Yanling Wei; Liang Chang; Dan Li; Liping Yang
Journal:  J Assist Reprod Genet       Date:  2013-02-03       Impact factor: 3.412

3.  A congenital cranial dysinnervation disorder: Möbius' syndrome.

Authors:  Hatice Mutlu Albayrak; Nuriye Tarakçı; Hüseyin Altunhan; Rahmi Örs; Hüseyin Çaksen
Journal:  Turk Pediatri Ars       Date:  2017-09-01

4.  Ten cases with 46,XX testicular disorder of sex development: single center experience.

Authors:  Emre Can Akinsal; Numan Baydilli; Abdullah Demirtas; Cetin Saatci; Oguz Ekmekcioglu
Journal:  Int Braz J Urol       Date:  2017 Jul-Aug       Impact factor: 1.541

5.  Molecular cytogenetic analysis and genetic counseling: a case report of eight 46,XX males and a literature review.

Authors:  Fagui Yue; Hongguo Zhang; Qi Xi; Yuting Jiang; Leilei Li; Ruizhi Liu; Ruixue Wang
Journal:  Mol Cytogenet       Date:  2019-11-04       Impact factor: 2.009

6.  46,XX male disorder of sexual development:a case report.

Authors:  Ahmet Anık; Gönül Çatlı; Ayhan Abacı; Ece Böber
Journal:  J Clin Res Pediatr Endocrinol       Date:  2013

7.  A newborn with ambiguous genitalia and a complex X;Y rearrangement.

Authors:  Mohammadreza Dehghani; Elena Rossi; Annalisa Vetro; Gianni Russo; Zahra Hashemian; Orsetta Zuffardi
Journal:  Iran J Reprod Med       Date:  2014-05

8.  A Korean boy with 46,XX testicular disorder of sex development caused by SOX9 duplication.

Authors:  Gyung Min Lee; Jung Min Ko; Choong Ho Shin; Sei Won Yang
Journal:  Ann Pediatr Endocrinol Metab       Date:  2014-06-30

9.  Sexual dimorphism in brain transcriptomes of Amami spiny rats (Tokudaia osimensis): a rodent species where males lack the Y chromosome.

Authors:  Madison T Ortega; Nathan J Bivens; Takamichi Jogahara; Asato Kuroiwa; Scott A Givan; Cheryl S Rosenfeld
Journal:  BMC Genomics       Date:  2019-01-25       Impact factor: 3.969

10.  Detection of SRY-positive46,XX male syndrome by the analysis of cell-free fetal DNA via non-invasive prenatal testing.

Authors:  Luigia De Falco; Giovanni Savarese; Teresa Suero; Sonia Amabile; Raffaella Ruggiero; Pasquale Savarese; Antonio Fico
Journal:  Clin Case Rep       Date:  2019-09-07
  10 in total

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