Concordance for Gender Dysphoria in Genetic Female Monozygotic (Identical) Triplets

Arch Sex Behav. 2022 Oct;51(7):3647-3651. doi: 10.1007/s10508-022-02409-1. Epub 2022 Aug 31.

Abstract

The biopsychosocial etiology of gender dysphoria is poorly understood, but current thought suggests a complex interaction of genetic, hormonal, environmental, and differences in brain development and physiology. Twin studies have implicated a genetic role in the formation of gender identity. Congruence for gender dysphoria is more common among monozygotic twins compared to dizygotic twins. We present a case of monozygotic (identical) triplets who have each transitioned from female to male under the care of a university transgender health service. Each triplet experienced gender dysphoria from childhood and has undergone transitional endocrine care and various aspects of gender-affirming surgery. Although a pure genetic or biological component cannot be attributed as a cause of their gender dysphoria with absolute certainty since the triplets were raised together, this unusual case of gender dysphoria among a set of monozygotic triplets adds support for a heritable role in gender identity formation.

Keywords: Gender dysphoria; Gender identity; Monozygotic; Transgender; Triplets.

Publication types

  • Case Reports

MeSH terms

  • Child
  • Female
  • Gender Dysphoria* / genetics
  • Gender Identity
  • Humans
  • Male
  • Transgender Persons*
  • Twins, Dizygotic / genetics
  • Twins, Monozygotic / genetics