Literature DB >> 2598069

[Familial testicular regression syndrome].

J Naffah.   

Abstract

The rare syndrome of embryonic testicular regression or agonadism with XY karyotype is described in this paper in a sibship of 7 including 3 cases of regression at a earlier time (in three amenorrheic sisters and on case of tardive and incomplete regression in a brother with bilateral testicular hypotrophy. The antigen H-Y is present in the three sisters. The pathogenesis of this syndrome, compared with that of pure gonadal dysgenesis is discussed.

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Year:  1989        PMID: 2598069

Source DB:  PubMed          Journal:  Bull Acad Natl Med        ISSN: 0001-4079            Impact factor:   0.144


  5 in total

1.  Mutational analysis of steroidogenic factor 1 (NR5a1) in 24 boys with bilateral anorchia: a French collaborative study.

Authors:  Pascal Philibert; Delphine Zenaty; Lin Lin; Sylvie Soskin; Françoise Audran; Juliane Léger; John C Achermann; Charles Sultan
Journal:  Hum Reprod       Date:  2007-10-16       Impact factor: 6.918

2.  Clinical, biological and genetic analysis of anorchia in 26 boys.

Authors:  Raja Brauner; Mathieu Neve; Slimane Allali; Christine Trivin; Henri Lottmann; Anu Bashamboo; Ken McElreavey
Journal:  PLoS One       Date:  2011-08-10       Impact factor: 3.240

Review 3.  Vanishing testes: a literature review.

Authors:  Özgür Pirgon; Bumin Nuri Dündar
Journal:  J Clin Res Pediatr Endocrinol       Date:  2012-09

4.  [Embryonic testicular regression syndrome: report of 6 cases].

Authors:  Hanane Latrech; Mohammed El Hassan Gharbi; Abdelmjid Chraïbi; Ahmed Gaouzi
Journal:  Pan Afr Med J       Date:  2014-07-26

5.  Pathogenic variants in the DEAH-box RNA helicase DHX37 are a frequent cause of 46,XY gonadal dysgenesis and 46,XY testicular regression syndrome.

Authors:  Ken McElreavey; Anne Jorgensen; Caroline Eozenou; Tiphanie Merel; Joelle Bignon-Topalovic; Daisylyn Senna Tan; Denis Houzelstein; Federica Buonocore; Nick Warr; Raissa G G Kay; Matthieu Peycelon; Jean-Pierre Siffroi; Inas Mazen; John C Achermann; Yuliya Shcherbak; Juliane Leger; Agnes Sallai; Jean-Claude Carel; Laetitia Martinerie; Romain Le Ru; Gerard S Conway; Brigitte Mignot; Lionel Van Maldergem; Rita Bertalan; Evgenia Globa; Raja Brauner; Ralf Jauch; Serge Nef; Andy Greenfield; Anu Bashamboo
Journal:  Genet Med       Date:  2019-07-24       Impact factor: 8.822

  5 in total

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