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Complete Androgen Insensitivity Syndrome: From Bench to Bed.


ABSTRACT: Complete androgen insensitivity syndrome (CAIS) is due to complete resistance to the action of androgens, determining a female phenotype in persons with a 46,XY karyotype and functioning testes. CAIS is caused by inactivating mutations in the androgen receptor gene (AR). It is organized in eight exons located on the X chromosome. Hundreds of genetic variants in the AR gene have been reported in CAIS. They are distributed throughout the gene with a preponderance located in the ligand-binding domain. CAIS mainly presents as primary amenorrhea in an adolescent female or as a bilateral inguinal/labial hernia containing testes in prepubertal children. Some issues regarding the management of females with CAIS remain poorly standardized (such as the follow-up of intact testes, the timing of gonadal removal and optimal hormone replacement therapy). Basic research will lead to the consideration of new issues to improve long-term well-being (such as bone health, immune and metabolic aspects and cardiovascular risk). An expert multidisciplinary approach is mandatory to increase the long-term quality of life of women with CAIS.

SUBMITTER: Tyutyusheva N 

PROVIDER: S-EPMC7865707 | biostudies-literature | 2021 Jan

REPOSITORIES: biostudies-literature

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Complete Androgen Insensitivity Syndrome: From Bench to Bed.

Tyutyusheva Nina N   Mancini Ilaria I   Baroncelli Giampiero Igli GI   D'Elios Sofia S   Peroni Diego D   Meriggiola Maria Cristina MC   Bertelloni Silvano S  

International journal of molecular sciences 20210127 3


Complete androgen insensitivity syndrome (CAIS) is due to complete resistance to the action of androgens, determining a female phenotype in persons with a 46,XY karyotype and functioning testes. CAIS is caused by inactivating mutations in the androgen receptor gene (<i>AR</i>). It is organized in eight exons located on the X chromosome. Hundreds of genetic variants in the <i>AR</i> gene have been reported in CAIS. They are distributed throughout the gene with a preponderance located in the ligan  ...[more]

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