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Fig. 1 | Orphanet Journal of Rare Diseases

Fig. 1

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

Fig. 1

Flowchart of grouping and follow-up. 5α-RD2, 5 alfa-reductase-2 deficiency; CAIS, complete androgen insensitivity syndrome; PAIS, partial androgen insensitivity syndrome; NR5A1, NR5AI gene mutation; CYP17A1, CYP17A1 gene mutation; PSAI, Pre-school Activities Inventory; CSRI, The Children's Sex Role Inventory; GD, gender dysphoria; DSM-5, diagnostic and statistical manual of mental disorders, 5th edition

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Orphanet Journal of Rare Diseases

ISSN: 1750-1172