Unidade de Endocrinologia do Desenvolvimento, Laboratorio de Hormonios e Genetica Molecular LIM42, Hospital das Clinicas da Faculdade de Medicina da Universidade de Sao Paulo, Av. Dr. Enéas de Carvalho Aguiar, 155, PAMB, 2º andar, Bloco 6, 05403-900 Sao Paulo, SP, Brazil.
Pediatr Nephrol. 2011 Aug;26(8):1311-5. doi: 10.1007/s00467-011-1847-4. Epub 2011 May 11.
WT1 mutations have been described in a variety of syndromes, including Denys-Drash syndrome (DDS), which is characterized by predisposition to Wilms' tumor, genital abnormalities and development of early nephropathy. The most frequent WT1 defects in DDS are missense mutations located in exons 8-9. Our aim is to report a novel WT1 mutation in a 46,XY patient with a DDS variant, who presented a mild nephropathy with a late onset diagnosed during adolescence. He had ambiguous genitalia at birth. At 4 months of age he underwent nephrectomy (Wilms' tumor) followed by chemotherapy. Ambiguous genitalia were corrected and bilateral gonadectomy was performed. Sequencing of WT1 identified a novel heterozygous mutation (c.742A>T) in exon 4 that generates a premature stop codon (p.K248X). Interestingly, this patient has an unusual DDS nephropathy progression, which reinforces that patients carrying WT1 mutations should have the renal function carefully monitored due to the possibility of late-onset nephropathy.
WT1 突变已在多种综合征中被描述,包括 Denys-Drash 综合征(DDS),其特征是易患肾母细胞瘤、生殖器异常和早期肾病的发生。DDS 中最常见的 WT1 缺陷是位于外显子 8-9 的错义突变。我们的目的是报告一例 DDS 变异的 46,XY 患者中 WT1 的新突变,该患者表现为轻度肾病,在青春期后诊断为迟发性。他出生时具有生殖器模糊。4 个月大时,他接受了肾切除术(肾母细胞瘤)和化疗。生殖器模糊得到纠正,并进行了双侧性腺切除术。WT1 的测序发现了一个新的杂合突变(c.742A>T)在外显子 4 中,导致提前终止密码子(p.K248X)。有趣的是,该患者具有不寻常的 DDS 肾病进展,这表明携带 WT1 突变的患者由于可能发生迟发性肾病,应仔细监测肾功能。