نتایج جستجو برای: androgen insensitivity syndrome

تعداد نتایج: 647111  

Journal: :Srpski arhiv za celokupno lekarstvo 2015

Journal: :international journal of fertility and sterility 0

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Journal: :journal of minimally invasive surgical sciences 0
saeed alborzi department of obstetrics and gynecology, shiraz university of medical sciences, shiraz, ir iran zohreh tavana laparoscopy research center, shiraz university of medical sciences, shiraz, ir iran; laproscoy research center, qadir hospital, quran avenue, p. o. box: 71345–1818, shiraz, ir iran. tel: +98–9173144462 madihe amini department of obstetrics and gynecology, shiraz university of medical sciences, shiraz, ir iran; laparoscopy research center, shiraz university of medical sciences, shiraz, ir iran

background the gonadectomy in patients with androgen insensitivity syndrome (ais) has been conventionally performed using laparotomic techniques. but currently several reports have suggested laparoscopic gonadectomy in these patients because of shorter hospital stay and minimal postoperative pain and hemorrhage. objective to report the laparoscopic gonadectomy in 11 patients suffering from andr...

Journal: :The Journal of clinical endocrinology and metabolism 2001
A L Boehmer O Brinkmann H Brüggenwirth C van Assendelft B J Otten M C Verleun-Mooijman M F Niermeijer H G Brunner C W Rouwé J J Waelkens W Oostdijk W J Kleijer T H van der Kwast M A de Vroede S L Drop

Androgen insensitivity syndrome encompasses a wide range of phenotypes, which are caused by numerous different mutations in the AR gene. Detailed information on the genotype/phenotype relationship in androgen insensitivity syndrome is important for sex assignment, treatment of androgen insensitivity syndrome patients, genetic counseling of their families, and insight into the functional domains...

2013
Marco Nezzo Pieter De Visschere Guy T'Sjoen Steven Weyers Geert Villeirs

Complete androgen insensitivity syndrome is an X-linked recessive androgen receptor disorder characterized by a female phenotype with an XY karyotype. Individuals affected by this syndrome have normal female external genitalia but agenesis of the Müllerian duct derivatives, that is, absence of the Fallopian tubes, uterus, cervix, and the proximal part of the vagina, with presence of endoabdomin...

Journal: :Archives of Endocrinology and Metabolism 2018

Journal: :The Lancet 1993
Ieuan A Hughes John D Davies Trevor I Bunch Vickie Pasterski Kiki Mastroyannopoulou Jane MacDougall

The androgen insensitivity syndromes (AIS) fall within the generic category of 46,XY DSD (disorder of sex development) and present as phenotypes associated with complete or partial resistance to the action of androgens. Three categories are recognized: complete androgen insensitivity syndrome (CAIS), partial androgen insensitivity syndrome (PAIS), mild androgen insensitivity syndrome (MAIS). Th...

2018
Mary F. Lyon Susan G. Hawkes

Androgen Insensitivity Syndrome (AIS) is a human disorder in which an individual's genetic sex (genotype) differs from that individual's observable secondary sex characteristics (phenotypes). A fetus [4] with AIS is genetically male with a 46,XY genotype. The term 46,XY refers to the chromosomes found in most cells of the fetus [4]. Most cells have a total of 46 autosomes, or non-sex chromosome...

2015

Androgen insensitivity syndrome (AIS) is a condition that results in the partial or complete inability of the cell to respond to androgens (androgenic hormones) that stimulate or control the development and maintenance of male physiological characteristics by binding to androgen receptors. The unresponsiveness of the cell to the presence of androgenic hormones can impair, or prevent, both the m...

Journal: :The Journal of Obstetrics and Gynecology of India 2012

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