Results 31 to 40 of about 30,274 (252)
Androgen insensitivity syndrome. [PDF]
Archives of Disease in Childhood, 1993 In a relatively short period of time, understanding of the fundamental causes of androgen insensitivity syndromes has improved dramatically. This has been brought about by the combination of several disciplines, including endocrinology, genetics, developmental and molecular biology. Mutations can be identified in the androgen receptor gene in suspected
Ieuan A. Hughes +2 more
openaire +4 more sources
MedPress Pediatrics and Child Health Care, 2022 We wish to present a very unusual case of an inheritance of a very rare disease, familial complete androgen insensitivity syndrome, in a baby girl with three mothers and the mother being a known case of complete androgen insensitive syndrome.
Neeva D. Govani +5 more
semanticscholar +1 more source
Challenges in the Diagnosis of XY Differences of Sexual Development
Medicina, 2022 Background: We report the clinical case of female patient with 46,XY difference of sexual development (DSD) and discuss the challenges in the differential diagnosis between complete gonadal dysgenesis (also called Swyer syndrome) and complete androgen ...
Žana Bumbulienė +5 more
doaj +1 more source
Complete androgen insensitivity syndrome and risk of gonadal malignancy: systematic review
Annals of Pediatric Endocrinology & Metabolism, 2021 Complete androgen insensitivity syndrome (CAIS) is a rare condition characterized by 46,XY karyotype, female external genitalia, absence of uterus, and testes located intra-abdominally, in the inguinal ring or in the labia majora.
B. A. Barros +5 more
semanticscholar +1 more source
Sexual Development, 2021 This study describes the clinical, biochemical, and molecular characteristics of Indian children with 46,XY DSD and suspected androgen insensitivity syndrome (AIS).
Anil Kumar +7 more
semanticscholar +1 more source
Androgen insensitivity syndrome.
European review for medical and pharmacological sciences, 2018 We provide a review of the literature about the Androgen Insensitivity Syndrome (AIS), its onset and associated developmental anomalies and the genetic alterations causing it.We searched PubMed with a larger emphasis on the physiology, genetics and current management of AIS.AIS is an X-linked recessive Disorder of Sex Development (DSD). It is caused by
Gulía, C +13 more
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Studia Medyczne, 2016 Androgen insensitivity syndrome (CAIS) – also called Morris syndrome, formerly known as testicular feminisation syndrome – is a congenital disorder of sex development caused by various mutations in the gene encoding the androgen receptor.
Przemysław Wolak
doaj +1 more source
Complete Androgen Insensitivity Syndrome [PDF]
The Journal of Obstetrics and Gynecology of India, 2012 Complete androgen insensitivity syndrome (AIS) is a medical condition which affects the development of the genital and reproductive system. This raises some very uncomfortable issues about gender identity that are difficult to put into words. The first medical report on AIS was published in 1953 by J. M. Morris, an American gynecologist.
Shilpa Chaudhari +2 more
openaire +3 more sources
A potential biomarker of androgen exposure in European bullhead (Cottus sp.) kidney [PDF]
Fish Physiology and Biochemistry 39, 3 (2013) 573-580, 2014 The aim of this study was to identify a signal that could be used as an androgen exposure indicator in the European bullhead (Cottus sp.). For this purpose, the ultra-structure of the kidney was characterized to identify normal structure of this organ, and histological changes previously described in the kidney of breeding male bullheads were ...
arxiv +1 more source
Androgen insensitivity syndrome.
Baillière's Clinical Endocrinology and Metabolism, 2019 In a relatively short period of time, understanding of the fundamental causes of androgen insensitivity syndromes has improved dramatically. This has been brought about by the combination of several disciplines, including endocrinology, genetics ...
H. Scharnagl +169 more
semanticscholar +1 more source