Complete androgen insensitivity (syndrome of Morris): A case

Authors

  • María Fajardo Instituto Materno Perinatal, Lima, Perú
  • Gloria Larrabure Instituto Materno Perinatal, Lima, Perú
  • Lic. Gamboa Instituto Materno Perinatal, Lima, Perú

DOI:

https://doi.org/10.31403/rpgo.v50i418

Abstract

Testicular feminization is a recessive genetic disorder linked to the X chromosome with complete androgen insensitivity, the most common form of male pseudohermaphroditism. The production of androgens by the testes is normal but there is no action for lack of receptors in the target organs. Individuals 46, XY show both testicles, female external genitals, vagina blind end and no miileriano derivative. The incidence is about 2 to 5 per 100,000, the phenotype is female. A catered event is presented in the Maternal Perinatal Institute in 2003, in the study and management who was for several specialties.

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Published

2015-05-05

How to Cite

Fajardo, M., Larrabure, G., & Gamboa, L. (2015). Complete androgen insensitivity (syndrome of Morris): A case. The Peruvian Journal of Gynecology and Obstetrics, 50(4), 209–211. https://doi.org/10.31403/rpgo.v50i418

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