Assessment of clinical scoring systems for the diagnosis of Williams-Beuren syndrome
Contribuinte(s) |
Universidade Estadual Paulista (UNESP) |
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Data(s) |
27/05/2014
27/05/2014
23/09/2013
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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 |