46,XY disorder of sex development caused by PPP1R12A gene variants: a case report.
10.7499/j.issn.1008-8830.2503003
- Author:
Wei SU
1
;
Zhe SU
1
;
Jing-Yu YOU
1
;
Hui-Ping SU
1
;
Li-Li PAN
1
;
Shu-Min FAN
1
;
Jian-Chun YIN
1
Author Information
1. Department of Endocrinology, Shenzhen Children's Hospital, Shenzhen, Guangdong 518038, China.
- Publication Type:English Abstract
- Keywords:
46,XY;
Child;
Disorder of sex development;
PPP1R12A gene;
Variant
- MeSH:
Humans;
Male;
Infant;
Disorder of Sex Development, 46,XY/etiology*;
Protein Phosphatase 1/genetics*
- From:
Chinese Journal of Contemporary Pediatrics
2025;27(8):1017-1021
- CountryChina
- Language:Chinese
-
Abstract:
The patient was a boy aged 1 year and 9 months who presented with 46,XY disorder of sex development (DSD), with severe undermasculinization of the external genitalia. Laboratory tests and ultrasound examinations showed normal functions of Leydig cells and Sertoli cells in the testes. Genetic testing revealed a novel pathogenic heterozygous variant, c.1186dupA (p.T396Nfs*17), in the PPP1R12A gene. Thirteen cases of PPP1R12A gene variants have been reported previously. These variants may cause isolated involvement of the genitourinary or neurological systems, or affect other systems/organs including the digestive tract, eyes, heart, etc. Patients with DSD typically present with a 46,XY karyotype and variable degrees of undermasculinization involving the external genitalia, gonads, and reproductive tract. This article reports a child with 46,XY DSD accompanied by growth retardation caused by a heterozygous variant in the PPP1R12A gene, which expands the clinical disease spectrum associated with PPP1R12A gene variants.
