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J Clin Res Pediatr Endocrinol ; 14(4): 469-474, 2022 12 01.
Artículo en Inglés | MEDLINE | ID: mdl-34355877

RESUMEN

The genetic cause of 46, XY disorder of sex development (DSD) still cannot be determined in about half of the cases. GATA-4 haploinsufficiency is one of the rare causes of DSD in genetic males (46, XY). Twenty-two cases with 46, XY DSD due to GATA-4 haploinsufficiency (nine missense variant, two copy number variation) have been previously reported. In these cases, the phenotype may range from a mild undervirilization to complete female external genitalia. The haploinsufficiency may be caused by a sequence variant or copy number variation (8p23 deletion). The aim of this study was to present two unrelated patients with DSD due to GATA-4 variants and to review the phenotypic and genotypic characteristics of DSD cases related to GATA-4 deficiency.


Asunto(s)
Trastorno del Desarrollo Sexual 46,XY , Factor de Transcripción GATA4 , Femenino , Humanos , Masculino , Trastorno del Desarrollo Sexual 46,XY/genética , Variaciones en el Número de Copia de ADN , Genotipo , Fenotipo , Desarrollo Sexual
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