alexa Androgen insensitivity syndrome.
Genetics

Genetics

Molecular Biology: Open Access

Author(s): Hughes IA, Davies JD, Bunch TI, Pasterski V, Mastroyannopoulou K,

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Abstract Androgen insensitivity syndrome in its complete form is a disorder of hormone resistance characterised by a female phenotype in an individual with an XY karyotype and testes producing age-appropriate normal concentrations of androgens. Pathogenesis is the result of mutations in the X-linked androgen receptor gene, which encodes for the ligand-activated androgen receptor--a transcription factor and member of the nuclear receptor superfamily. This Seminar describes the clinical manifestations of androgen insensitivity syndrome from infancy to adulthood, reviews the mechanism of androgen action, and shows examples of how mutations of the androgen receptor gene cause the syndrome. Management of androgen insensitivity syndrome should be undertaken by a multidisciplinary team and include gonadectomy to avoid gonad tumours in later life, appropriate sex-hormone replacement at puberty and beyond, and an emphasis on openness in disclosure. Copyright © 2012 Elsevier Ltd. All rights reserved. This article was published in Lancet and referenced in Molecular Biology: Open Access

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