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


Autoria(s): Leme, D. E S; Souza, D. H.; Mercado, G.; Pastene, E.; Dias, Adriano; Moretti-Ferreira, D.
Contribuinte(s)

Universidade Estadual Paulista (UNESP)

Data(s)

27/05/2014

27/05/2014

23/09/2013

Resumo

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. © FUNPEC-RP.

Formato

3407-3411

Identificador

http://dx.doi.org/10.4238/2013.September.4.7

Genetics and Molecular Research, v. 12, n. 3, p. 3407-3411, 2013.

1676-5680

http://hdl.handle.net/11449/76625

10.4238/2013.September.4.7

WOS:000331717400131

2-s2.0-84884226340

2-s2.0-84884226340.pdf

Idioma(s)

eng

Relação

Genetics and Molecular Research

Direitos

openAccess

Palavras-Chave #Chromosome 7 #Clinical diagnosis #Elastin (ELN) gene #Fluorescence in situ hybridization #Williams-Beuren syndrome
Tipo

info:eu-repo/semantics/article