A familial WT1 mutation associated with incomplete Denys-Drash syndrome

作者：Zhu Chunhua; Zhao Fei; Zhang Weizhen; Wu Hongmei; Chen Ying; Ding Guixia; Zhang Aihua; Huang Songming^*

来源：European Journal of Pediatrics, 2013, 172(10): 1357-1362.

DOI：10.1007/s00431-013-2004-9

• WT1 gene mutation
• Denys-Drash syndrome
• Children
• Family
• Frasier syndrome

Denys-Drash syndrome (DDS) is a rare disorder characterized by nephropathy, male pseudohermaphroditism, and wilms tumor. Cases are thought to arise sporadically through a de novo mutation in the wilms tumor suppressor gene (WT1), which encodes a zinc finger protein that not only acts as a tumor suppressor but is essential for normal gonadogenesis, nephrogenesis, and development of the urogenital tract. In this report, we describe a family with the well-known missense mutation in exon 9 of the WT1 gene, 1180C > T (R394W), causing incomplete DDS and no symptoms in their father. The proband, a boy with 46, XY karyotype, was born with ambiguous genitalia, penoscrotal hypospadias, and bilateral inguinal hernias. At 2 years of age, he has proteinuria and diffuse mesangial sclerosis, but no wilms tumor has been detected. The elder sister of the proband, at 3 years of age, has normal genitalia, proteinuria, focal mesangial sclerosis but no wilms tumor. The WT1 mutation was detected in both patients, who have suspected DDS, and their father, who is phenotypically normal. Conclusion: This case is unusual in that the 1180C > T mutation, which has been found in approximately 50 % of patients with complete DDS, has been inherited and is causing mild or no symptoms of DDS.

• 出版日期2013-10
• 单位南京医科大学