GATA-4 Variants in Two Unrelated Cases with 46, XY Disorder of Sex Development and Review of the Literature

Küçük Resim Yok

Tarih

2022

Dergi Başlığı

Dergi ISSN

Cilt Başlığı

Yayıncı

Galenos Publishing House

Erişim Hakkı

info:eu-repo/semantics/openAccess

Özet

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-4variants and to review the phenotypic and genotypic characteristics of DSD cases related to GATA-4 deficiency. © 2022 by Turkish Society for Pediatric Endocrinology and Diabetes.

Açıklama

Anahtar Kelimeler

Disorder of sex development; GATA-4; Gonad; heart

Kaynak

JCRPE Journal of Clinical Research in Pediatric Endocrinology

WoS Q Değeri

Scopus Q Değeri

Q2

Cilt

14

Sayı

4

Künye