一种新型变异导致WT1相关的性综合征和性别发育的差异:一个病例报告

Shan Gao1, Dahai Wang1, Xingmei Ding2

  • 1Department of Pediatric Nephrology, Rheumatology and Immunology, The Affiliated Hospital of Qingdao University, Qingdao, China.

Frontiers in pediatrics
|September 22, 2025
PubMed
概括

威尔姆斯瘤基因1 (WT1) 的新型突变在患有瘤综合征和性别发育差异的患者中被确定. 这一发现扩大了已知的WT1基因变异,并改善了对相关疾病的理解.

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