Literature DB >> 24065682

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

D E S Leme1, D H Souza, G Mercado, E Pastene, A Dias, D Moretti-Ferreira.   

Abstract

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.

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Year:  2013        PMID: 24065682     DOI: 10.4238/2013.September.4.7

Source DB:  PubMed          Journal:  Genet Mol Res        ISSN: 1676-5680


  4 in total

1.  8p deletion is strongly linked to poor prognosis in breast cancer.

Authors:  P Lebok; A Mittenzwei; M Kluth; C Özden; B Taskin; K Hussein; K Möller; A Hartmann; A Lebeau; I Witzel; S Mahner; L Wölber; F Jänicke; S Geist; P Paluchowski; C Wilke; U Heilenkötter; R Simon; G Sauter; L Terracciano; R Krech; A von der Assen; V Müller; E Burandt
Journal:  Cancer Biol Ther       Date:  2015-05-11       Impact factor: 4.742

2.  Clinical application of chromosomal microarray analysis for the diagnosis of Williams-Beuren syndrome in Chinese Han patients.

Authors:  Yu Xia; Shufang Huang; Yueheng Wu; Yongchao Yang; Shaoxian Chen; Ping Li; Jian Zhuang
Journal:  Mol Genet Genomic Med       Date:  2018-12-18       Impact factor: 2.183

3.  Proposed criteria for nevoid basal cell carcinoma syndrome in children assessed using statistical optimization.

Authors:  Nina B Gold; Ian M Campbell; Sarah E Sheppard; Wen-Hann Tan
Journal:  Sci Rep       Date:  2021-10-05       Impact factor: 4.379

4.  Diagnostic Path of a Genetic Disease: A Case of Williams-Beuren Syndrome in Burkina Faso.

Authors:  Makoura Barro; Bintou Sanogo; Aimée S Kissou; Ad Bafa Ibrahim Ouattara; Boubacar Nacro
Journal:  Pediatr Rep       Date:  2015-12-17
  4 in total

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