Literature DB >> 25666240

A rare cause of primary amenorrhoea, the XY female with gonadal dysgenesis.

Dominique Mannaerts1, Joke Muys1, Bettina Blaumeiser1, Yves Jacquemyn2.   

Abstract

Disorders of sexual development are conditions where sexual phenotype and genotype are discordant. Genetic sex is determined at conception as the ovum is fertilised by a spermatozoon that contains either an X or Y chromosome. A complex pathway determined by genes and hormones leads to gonadal differentiation into testis or ovary and promotes the development of internal and external genitalia. We present a case of an 18-year-old woman who presented with primary amenorrhoea. She was a virgin, and apart from hirsutism and overweight, had no complaints. Her family history was insignificant. The patient was tall and had underdeveloped breasts. Her blood results showed hypergonadotropic hypogonadism. A 46, XY genotype was detected with karyotype analysis. Ultrasound and MRI demonstrated the presence of a uterus, but no overt gonads. Laparoscopy was performed, with bilateral removal of streak ovaries. 2015 BMJ Publishing Group Ltd.

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Mesh:

Year:  2015        PMID: 25666240      PMCID: PMC4330456          DOI: 10.1136/bcr-2014-206609

Source DB:  PubMed          Journal:  BMJ Case Rep        ISSN: 1757-790X


  5 in total

1.  The XY female.

Authors:  Lina Michala; Sarah M Creighton
Journal:  Best Pract Res Clin Obstet Gynaecol       Date:  2009-11-06       Impact factor: 5.237

2.  A novel mutation (c. 341A>G) in the SRY gene in a 46,XY female patient with gonadal dysgenesis.

Authors:  Zofia Helszer; Anita Dmochowska; Janusz Szemraj; Jolanta Słowikowska-Hilczer; Marek Wieczorek; Sławomir Jędrzejczyk; Bogdan Kałużewski
Journal:  Gene       Date:  2013-04-24       Impact factor: 3.688

3.  Global gene profiling and comprehensive bioinformatics analysis of a 46,XY female with pericentric inversion of the Y chromosome.

Authors:  Tomoko Mitsuhashi; Katsuhiko Warita; Yoshiaki Tabuchi; Ichiro Takasaki; Takashi Kondo; Teruo Sugawara; Fumio Hayashi; Zhi-Yu Wang; Yoshiki Matsumoto; Takanori Miki; Yoshiki Takeuchi; Yasuhiko Ebina; Hideto Yamada; Noriaki Sakuragi; Toshifumi Yokoyama; Takashi Nanmori; Hiroshi Kitagawa; Jeffrey A Kant; Nobuhiko Hoshi
Journal:  Congenit Anom (Kyoto)       Date:  2010-03       Impact factor: 1.409

4.  Steroidogenic factor-1 (SF-1) gene mutation as a frequent cause of primary amenorrhea in 46,XY female adolescents with low testosterone concentration.

Authors:  Pascal Philibert; Elodie Leprieur; Delphine Zenaty; Elisabeth Thibaud; Michel Polak; Anne-Marie Frances; James Lespinasse; Isabelle Raingeard; Nadège Servant; Françoise Audran; Françoise Paris; Charles Sultan
Journal:  Reprod Biol Endocrinol       Date:  2010-03-19       Impact factor: 5.211

Review 5.  Care of women with XY karyotype: a clinical practice guideline.

Authors:  Pernille Bach Jorgensen; Kristín Rós Kjartansdóttir; Jens Fedder
Journal:  Fertil Steril       Date:  2009-04-09       Impact factor: 7.329

  5 in total
  1 in total

1.  Complete gonadal dysgenesis analysis in the population of Latvia: malignant outcomes and a review of literature.

Authors:  Alise Jakovleva; Zanna Kovalova
Journal:  Med Pharm Rep       Date:  2022-01-31
  1 in total

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