Literature DB >> 7400886

Embryonic testicular regression syndrome: variable phenotypic expression in siblings.

N Josso, M L Briard.   

Abstract

Two 46,XY agonadal siblings with variable degrees of sexual ambiguity are described. The eldest child is a phenotypic male with micropenis. The younger patient, a phenotypic female with slight fusion of the genital folds and absent müllerian ducts, conforms to the criteria usually accepted for the diagnosis of true agonadism. Coexistence of anorchia and true agonadism in the same sibship supports the hypothesis, suggested by others, that both disorders are related and are due to the regression of the embryonic testes.

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Year:  1980        PMID: 7400886     DOI: 10.1016/s0022-3476(80)80474-4

Source DB:  PubMed          Journal:  J Pediatr        ISSN: 0022-3476            Impact factor:   4.406


  10 in total

Review 1.  Etiopathogenesis, classification, investigations and diagnosis in intersex disorders.

Authors:  M G Forest
Journal:  Indian J Pediatr       Date:  1992 Jul-Aug       Impact factor: 1.967

Review 2.  To 'Pex or Not to 'Pex: What to Do for the Contralateral Testis When a Nubbin Is Discovered.

Authors:  John E Kehoe; Matthew S Christman
Journal:  Curr Urol Rep       Date:  2017-02       Impact factor: 3.092

3.  Mapping the testis determinants by an analysis of Y-specific sequences in males with apparent XX and XO karyotypes and females with XY karyotypes.

Authors:  N A Affara; M A Ferguson-Smith; R E Magenis; J L Tolmie; E Boyd; A Cooke; D Jamieson; K Kwok; M Mitchell; L Snadden
Journal:  Nucleic Acids Res       Date:  1987-09-25       Impact factor: 16.971

4.  Testicular degeneration in three patients with the persistent müllerian duct syndrome.

Authors:  S Imbeaud; R Rey; P Berta; J L Chaussain; J M Wit; R H Lustig; M A De Vroede; J Y Picard; N Josso
Journal:  Eur J Pediatr       Date:  1995-03       Impact factor: 3.183

5.  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

6.  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

7.  Familial forms of disorders of sex development may be common if infertility is considered a comorbidity.

Authors:  Raja Brauner; Flavia Picard-Dieval; Henri Lottmann; Sébastien Rouget; Joelle Bignon-Topalovic; Anu Bashamboo; Ken McElreavey
Journal:  BMC Pediatr       Date:  2016-11-29       Impact factor: 2.125

8.  The Evaluation of Cases with Y-Chromosome Gonadal Dysgenesis: Clinical Experience over 18 Years.

Authors:  Merih Berberoğlu; Zeynep Şıklar
Journal:  J Clin Res Pediatr Endocrinol       Date:  2017-08-21

Review 9.  Vanishing testes: a literature review.

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

10.  [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
  10 in total

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