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Related Experiment Video

Updated: Apr 21, 2026

Establishment of Rat Models Mimicking Gender-affirming Hormone Therapies
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Androgen insensitivity syndrome.

Rieko Tadokoro-Cuccaro1, Ieuan A Hughes

  • 1Department of Paediatrics, Addenbrooke's Hospital, University of Cambridge, Cambridge, UK.

Current Opinion in Endocrinology, Diabetes, and Obesity
|October 30, 2014
PubMed
Summary

Androgen insensitivity syndrome (AIS) management requires a multidisciplinary approach. This review updates clinical and genetic aspects, focusing on outcomes and gonadal tumor risks in complete and partial AIS.

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Area of Science:

  • Endocrinology
  • Genetics
  • Reproductive Medicine

Background:

  • Androgen insensitivity syndrome (AIS) presents diverse phenotypes.
  • Management necessitates a multidisciplinary strategy from infancy through adulthood.

Purpose of the Study:

  • To provide an updated review of clinical and genetic aspects of AIS.
  • To present outcome data on surgical and psychosexual findings.
  • To discuss the risk of gonadal tumors in AIS patients.

Main Methods:

  • Literature review of clinical features, genetic mutations, and long-term outcomes.
  • Analysis of recent trends in sex of rearing.
  • Inclusion of surgical and psychosexual findings.

Main Results:

  • Review covers clinical features and genetic aspects of androgen receptor gene mutations.
  • Longer-term outcomes for complete and partial AIS are discussed.
  • Trends in sex of rearing are examined.

Conclusions:

  • Further follow-up studies are essential for optimizing AIS management, particularly for partial forms.
  • Accurate prediction of gonadal tumor risk is crucial for gonadectomy decisions.