Leme D E S, Souza D H, Mercado G, Pastene E, Dias A, Moretti-Ferreira D
Serviço de Aconselhamento Genético, Departamento de Genética, Instituto de Biociências de Botucatu, Universidade Estadual Paulista, Botucatu, SP, Brasil.
Genet Mol Res. 2013 Sep 4;12(3):3407-11. doi: 10.4238/2013.September.4.7.
Williams-Beuren syndrome (WBS) is a genetic disorder characterized by physical and intellectual developmental delay, associated with congenital heart disease and facial dysmorphism. WBS is caused by a microdeletion on chromosome 7 (7q11.23), which encompasses the elastin (ELN) gene and about 27 other genes. The gold standard for WBS laboratory diagnosis is FISH (fluorescence in situ hybridization), which is very costly. As a possible alternative, we investigated the accuracy of three clinical diagnostic scoring systems in 250 patients with WBS diagnosed by FISH. We concluded that all three systems could be used for the clinical diagnosis of WBS, but they all gave a low percentage of false-positive (6.0-9.2%) and false-negative (0.8-4.0%) results. Therefore, their use should be associated with FISH testing.
威廉姆斯-贝伦综合征(WBS)是一种遗传性疾病,其特征为身体和智力发育迟缓,伴有先天性心脏病和面部畸形。WBS由7号染色体(7q11.23)上的微缺失引起,该区域包含弹性蛋白(ELN)基因和大约27个其他基因。WBS实验室诊断的金标准是荧光原位杂交(FISH),其成本非常高。作为一种可能的替代方法,我们在250例经FISH诊断为WBS的患者中研究了三种临床诊断评分系统的准确性。我们得出结论,所有这三种系统都可用于WBS的临床诊断,但它们的假阳性(6.0-9.2%)和假阴性(0.8-4.0%)结果比例都很低。因此,它们的使用应与FISH检测相结合。