Literature DB >> 27998513

Sexual orientation and medical history among Iranian people with Complete Androgen Insensitivity Syndrome and Congenital Adrenal Hyperplasia.

Behzad S Khorashad1, Ghasem M Roshan2, Alistair G Reid3, Zahra Aghili4, Mehran Hiradfar5, Mozhgan Afkhamizadeh6, Ali Talaei7, Azadeh Aarabi8, Nosrat Ghaemi9, Negin Taghehchian10, Hedieh Saberi11, Nazanin Farahi12, Mohammad Reza Abbaszadegan13.   

Abstract

OBJECTIVE: To report sexual orientation, relationship status and medical history of Iranian people with Differences of Sex Development (DSD) who were raised female.
METHODS: Our participants consisted of nineteen 46,XY individuals with Complete Androgen Insensitivity Syndrome (CAIS) and eighteen 46,XX individuals with Congenital Adrenal Hyperplasia (CAH) who were raised as females and older than 13years. As well as their relationship status and detailed medical history, an expert psychiatrist assessed their sexual orientation by a semi-structured psychiatric interview with them and, where applicable, their parents.
RESULTS: Five percent of CAH participants and 42% of CAIS participants were in a relationship, which was significantly different. All CAH individuals had been diagnosed at birth; 89% of CAIS had been diagnosed after puberty and due to primary amenorrhea and 11% were diagnosed in childhood due to inguinal hernia. Genital reconstructive surgery had been performed in 100% of CAH participants and 37% of CAIS. Regarding sexual contact experiences and sexual fantasies (androphilic, gynephilic or both), no significant differences were found. However, CAH females had significantly more gynephilic dreams (P=0.045).
CONCLUSION: This study, notable as one of the rare from a non-western culture, described sexual, medical and socioeconomic status of 46,XX CAH and 46,XY CAIS individuals living in Iran. Although broadly in line with previous findings from Western cultures, Iranian CAH individuals had fewer romantic relationships, but in contrast to previous studies their sexual orientation was only different from CAIS in the contents of sexual dreams.
Copyright © 2016 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Complete Androgen Insensitivity Syndrome; Congenital Adrenal Hyperplasia; Disorders of sexual development; Sexual orientation

Mesh:

Year:  2016        PMID: 27998513     DOI: 10.1016/j.jpsychores.2016.12.002

Source DB:  PubMed          Journal:  J Psychosom Res        ISSN: 0022-3999            Impact factor:   3.006


  4 in total

1.  The role of ultrasound to evaluate the disorders of sex development: a pictorial essay.

Authors:  Takahiro Hosokawa; Yutaka Tanami; Yumiko Sato; Mayumi Hosokawa; Eiji Oguma
Journal:  J Ultrasound       Date:  2022-01-06

2.  Androgen Insensitivity Syndrome: A rare genetic disorder.

Authors:  Sushrut Fulare; Satish Deshmukh; Jyoti Gupta
Journal:  Int J Surg Case Rep       Date:  2020-02-06

3.  One hundred twelve cases of 46, XY DSD patients after initial gender assignment: a short-term survey of gender role and gender dysphoria.

Authors:  Liping Hou; Ming Zhao; Lijun Fan; Bingyan Cao; Jiajia Chen; Yonghua Cui; Michel Polak; Chunxiu Gong
Journal:  Orphanet J Rare Dis       Date:  2021-10-09       Impact factor: 4.303

4.  2D:4D Suggests a Role of Prenatal Testosterone in Gender Dysphoria.

Authors:  Mostafa Sadr; Behzad S Khorashad; Ali Talaei; Nasrin Fazeli; Johannes Hönekopp
Journal:  Arch Sex Behav       Date:  2020-01-23
  4 in total

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