hrp0095p1-574 | Sex Differentiation, Gonads and Gynaecology, and Sex Endocrinology | ESPE2022
Kaninde Abhidhamma
, Baranowski Elizabeth
, Igbowke Rebecca
, McCarthy Liam
, Chandran Harish
, Vandermerwe Elmarie
, Fulton Piers
, Godber Caroline
, Smart Helen
, Curtis Joanne
, Cole Trevor
, Gleeson Helena
, Latthe Pallavi
, Kirk Jeremy
, Idkowiak Jan
, Mohamed Zainaba
Background: 5α-reductase type 2 deficiency (SRD5A2) is a rare cause of 46,XY DSD. Consensus guidelines on sex of rearing assignment at birth favours male gender. Typically undervirilised genitalia at birth virilise variably at puberty, posing gender identity challenges.Aim: We describe relevant data on clinical phenotype, hormonal and molecular workup and gender preference in patients with SRD5A2 deficiency from a ...