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Androgen insensitivity in forty-nine patients: Classification based on clinical and androgen receptor phenotypes

, 1987
Androgen receptor binding was studied in genital skin fibroblasts from 49 patients with androgen insensitivity syndrome (AIS) classified as complete (CAIS) or partial (PAIS) based on the clinical phenotype.
Hughes, I. A., Evans, Bronwen Alice James +1 more
core +1 more source

Three siblings with complete androgen insensitivity syndrome [PDF]

, 2013
A 27-year old woman presented with primary amenorrhoea and infertility. On examination, she was found to have palpable inguinal gonads, normal female external genitalia, a blind-ending vagina with no cervix, almost complete absence of axillary and pubic ...
Kemp, T
core

A Case of Complete Androgen Insensitivity Syndrome [PDF]

, 2009
Androgen insensitivity syndrome, gonadectomy, estrogen supplementation a 23-year-old single female visited our gynecological clinic because of primary amenorrhea. The patient's breast development was good.
内藤, 愼二 +4 more
core

Androgen Insensitivity Syndrome: A Case Report of Clinical Intricacies [PDF]

Testicular Feminisation Syndrome, commonly termed as Androgen Insensitivity Syndrome (AIS), is a very uncommon genetic disorder. Although AIS patients are genetically male (46, XY), they may have all or some of the physical characteristics of females ...
R. Sahasra Serisha, Ganesh Guru
core +1 more source

Complete androgen insensitivity syndrome with cryptorchid sertoli cell tumor: a case report and literature review [PDF]

Yuqing Wang +5 more
openalex +1 more source

LINE1-mediated epigenetic repression of androgen receptor transcription causes androgen insensitivity syndrome

Scientific Reports
Androgen insensitivity syndrome (AIS) is a difference of sex development (DSD) characterized by different degrees of undervirilization in individuals with a 46,XY karyotype despite normal to high gonadal testosterone production.
Jelena Pozojevic +14 more
doaj +1 more source

Case Report: Clinical and molecular genetic analysis of a patient with coexisting complete androgen insensitivity syndrome and neurofibromatosis type 1 and 15pstk + polymorphism [PDF]