Literature DB >> 19896906

The XY female.

Lina Michala1, Sarah M Creighton.   

Abstract

Sexual differentiation depends upon a series of complex events that leads to the differentiation of gonads into testicular tissue and the production and action of androgens on genital tissue. Variations in any of the pathways affecting the above events can lead into conditions where the phenotype and genotype are discordant, conditions nowadays called disorders of sex development (DSDs). These conditions may have some aspects in common such as infertility and the need for feminising surgery or gonadectomy. However, each entity has its particularities, and it is necessary that every effort is made to reach the correct diagnosis. As genetic information becomes more readily available, these conditions can be diagnosed with more ease and appropriate counselling can be provided to other members of the family regarding the treatment options and risk. Due to the rarity of DSDs, it is important that their management is undertaken in tertiary referral centres with accumulated experience on diagnosis and management and where a multidisciplinary team can provide the necessary medical and surgical support. Disclosure of the diagnosis should be done in a sensitive way by experienced staff, and psychological counselling should be readily available to patients and their family. Copyright 2009 Elsevier Ltd. All rights reserved.

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Year:  2009        PMID: 19896906     DOI: 10.1016/j.bpobgyn.2009.09.009

Source DB:  PubMed          Journal:  Best Pract Res Clin Obstet Gynaecol        ISSN: 1521-6934            Impact factor:   5.237


  6 in total

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

Authors:  Dominique Mannaerts; Joke Muys; Bettina Blaumeiser; Yves Jacquemyn
Journal:  BMJ Case Rep       Date:  2015-02-09

2.  Female with 46, XY karyotype.

Authors:  Eun Jung Jung; Do Hwa Im; Yong Hee Park; Jung Mi Byun; Young Nam Kim; Dae Hoon Jeong; Moon Su Sung; Ki Tae Kim; Hyo Jung An; Soo Jin Jung; Kyung Bok Lee
Journal:  Obstet Gynecol Sci       Date:  2017-07-14

3.  Case report of whole genome sequencing in the XY female: identification of a novel SRY mutation and revision of a misdiagnosis of androgen insensitivity syndrome.

Authors:  Sunita M C De Sousa; Karin S Kassahn; Liam C McIntyre; Chan-Eng Chong; Hamish S Scott; David J Torpy
Journal:  BMC Endocr Disord       Date:  2016-11-08       Impact factor: 2.763

4.  Case Report: Is It Premature Ovarian Insufficiency or Swyer Syndrome After Bone Marrow Transplantation?

Authors:  Hui Li; Jin Li; Xiaohong Li; Hong Yi; Qixiu Ren; Xiaoyan Chen
Journal:  Front Pediatr       Date:  2022-01-13       Impact factor: 3.418

5.  State of the art review in gonadal dysgenesis: challenges in diagnosis and management.

Authors:  Bonnie McCann-Crosby; Roshanak Mansouri; Jennifer E Dietrich; Laurence B McCullough; V Reid Sutton; Elise G Austin; Bruce Schlomer; David R Roth; Lefkothea Karaviti; Sheila Gunn; M John Hicks; Charles G Macias
Journal:  Int J Pediatr Endocrinol       Date:  2014-04-14

6.  Diagnostic laparoscopy in a twelve year old girl with right iliac fossa pain: A life changing diagnosis of complete androgen insensitivity syndrome.

Authors:  Babak Meshkat; Melania Matcovici; Claire Buckley; Muhammad Salama; Haresh K Perthiani
Journal:  Int J Surg Case Rep       Date:  2014-06-12
  6 in total

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