Assessment of clinical scoring systems for the diagnosis of Williams-Beuren syndrome

• Published in: Genetics and molecular research Vol. 12; no. 3; pp. 3407 - 3411
• Main Authors: Leme, D E S, Souza, D H, Mercado, G, Pastene, E, Dias, A, Moretti-Ferreira, D
• Format: Journal Article
• Language: English
• Published: Brazil 04.09.2013
• Subjects: Chromosome Deletion; Chromosomes, Human, Pair 7 - genetics; Elastin - genetics; Female; Humans; In Situ Hybridization, Fluorescence; Male; Research Design - standards; Williams Syndrome - diagnosis; Williams Syndrome - genetics; Williams Syndrome - pathology
• ISSN: 1676-5680
• 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.