Prolonged anorexia nervosa associated with female-to-male gender dysphoria: A case report

Transsexual (TS) individuals seem to display an increased risk in having eating disorders. Several case reports describe TS individuals with anorexia nervosa (AN). In order to understand better the impact of gender dysphoria (GD) and hormonal/surgical treatments on the occurrence and course of eatin...

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Veröffentlicht in:Eating behaviors : an international journal 2015-08, Vol.18, p.54-56
Hauptverfasser: Turan, Şenol, Poyraz, Cana Aksoy, Duran, Alaattin
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container_title Eating behaviors : an international journal
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creator Turan, Şenol
Poyraz, Cana Aksoy
Duran, Alaattin
description Transsexual (TS) individuals seem to display an increased risk in having eating disorders. Several case reports describe TS individuals with anorexia nervosa (AN). In order to understand better the impact of gender dysphoria (GD) and hormonal/surgical treatments on the occurrence and course of eating disorders in TS patients long term follow-up studies are needed. We present here a 41-year-old female-to-male TS patient suffering from AN. History revealed that pathological eating habits could strongly be associated with her GD. Hormonal and surgical treatments resulted in substantial improvement in the given eating disorder. The impact of GD on the development and treatment of eating disorder is discussed in this report. •İndividuals with GD may be at risk for subclinical eating disorders.•The impact of hormonal treatment appears to be substantial in alleviating symptoms of disordered eating in individuals with GD.•FtM and MtF transsexuals may have different motives to lose weight although the body dissatisfaction is the major common aspect.
doi_str_mv 10.1016/j.eatbeh.2015.03.012
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subjects Adult
Anorexia Nervosa - diagnosis
Eating disorder
Feeding Behavior - psychology
Female
Gender dysphoria
Humans
Male
Risk Assessment
Transgender Persons - psychology
Transgender Persons - statistics & numerical data
Transsexual
title Prolonged anorexia nervosa associated with female-to-male gender dysphoria: A case report
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