Assessment of clinical scoring systems for the diagnosis of Williams-Beuren syndrome
- Autores
- Leme, D E S; Souza, D H; Mercado, Graciela; Pastene, E. A.; Dias, A; Moretti-Ferreira, D
- Año de publicación
- 2013
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- Fil: Leme, D. E. S. Universidade Estadual Paulista. Instituto de Biociencias de Botucatu. Departamento de Genética. Servico de Aconselhamento Genético; Brasil.
Fil: Souza, D. H. Universidade Estadual Paulista. Instituto de Biociencias de Botucatu. Departamento de Genética. Servico de Aconselhamento Genético; Brasil.
Fil: Mercado, Graciela. ANLIS Dr.C.G.Malbrán. Centro Nacional de Genética Médica; Argentina.
Fil: Pastene, E. ANLIS Dr.C.G.Malbrán. Centro Nacional de Genética Médica; Argentina.
Fil: Dias, A. Universidade Estadual Paulista. Faculdade de Medicina de Botucatu. Departamento de Saúde Pública; Brasil.
Fil: Moretti-Ferreira, D. Universidade Estadual Paulista. Instituto de Biociencias de Botucatu. Departamento de Genética. Servico de Aconselhamento Genético; Brasil.
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. - Materia
-
Síndrome de Williams
Hibridación Fluorescente in Situ
Cromosomas Humanos Par 7 - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- Repositorio
- Institución
- Administración Nacional de Laboratorios e Institutos de Salud "Dr. Carlos G. Malbrán"
- OAI Identificador
- oai:sgc.anlis.gob.ar:Publications/123456789/1966
Ver los metadatos del registro completo
id |
SGCANLIS_bb2b150647e1519216507e67c5f8e1e8 |
---|---|
oai_identifier_str |
oai:sgc.anlis.gob.ar:Publications/123456789/1966 |
network_acronym_str |
SGCANLIS |
repository_id_str |
a |
network_name_str |
Sistema de Gestión del Conocimiento ANLIS MALBRÁN |
spelling |
Assessment of clinical scoring systems for the diagnosis of Williams-Beuren syndromeLeme, D E SSouza, D HMercado, GracielaPastene, E. A.Dias, AMoretti-Ferreira, DSíndrome de WilliamsHibridación Fluorescente in SituCromosomas Humanos Par 7Fil: Leme, D. E. S. Universidade Estadual Paulista. Instituto de Biociencias de Botucatu. Departamento de Genética. Servico de Aconselhamento Genético; Brasil.Fil: Souza, D. H. Universidade Estadual Paulista. Instituto de Biociencias de Botucatu. Departamento de Genética. Servico de Aconselhamento Genético; Brasil.Fil: Mercado, Graciela. ANLIS Dr.C.G.Malbrán. Centro Nacional de Genética Médica; Argentina.Fil: Pastene, E. ANLIS Dr.C.G.Malbrán. Centro Nacional de Genética Médica; Argentina.Fil: Dias, A. Universidade Estadual Paulista. Faculdade de Medicina de Botucatu. Departamento de Saúde Pública; Brasil.Fil: Moretti-Ferreira, D. Universidade Estadual Paulista. Instituto de Biociencias de Botucatu. Departamento de Genética. Servico de Aconselhamento Genético; Brasil.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.2013-09-04info:ar-repo/semantics/articuloinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://www.geneticsmr.com/articles/2399http://sgc.anlis.gob.ar/handle/123456789/1966https://doi.org/10.4238/2013.September.4.7Genetics and molecular researchenginfo:eu-repo/semantics/openAccessreponame:Sistema de Gestión del Conocimiento ANLIS MALBRÁNinstname:Administración Nacional de Laboratorios e Institutos de Salud "Dr. Carlos G. Malbrán"instacron:ANLIS2025-09-04T11:18:01Zoai:sgc.anlis.gob.ar:Publications/123456789/1966Institucionalhttp://sgc.anlis.gob.ar/Organismo científico-tecnológicoNo correspondehttp://sgc.anlis.gob.ar/oai/biblioteca@anlis.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:a2025-09-04 11:18:01.706Sistema de Gestión del Conocimiento ANLIS MALBRÁN - Administración Nacional de Laboratorios e Institutos de Salud "Dr. Carlos G. Malbrán"false |
dc.title.none.fl_str_mv |
Assessment of clinical scoring systems for the diagnosis of Williams-Beuren syndrome |
title |
Assessment of clinical scoring systems for the diagnosis of Williams-Beuren syndrome |
spellingShingle |
Assessment of clinical scoring systems for the diagnosis of Williams-Beuren syndrome Leme, D E S Síndrome de Williams Hibridación Fluorescente in Situ Cromosomas Humanos Par 7 |
title_short |
Assessment of clinical scoring systems for the diagnosis of Williams-Beuren syndrome |
title_full |
Assessment of clinical scoring systems for the diagnosis of Williams-Beuren syndrome |
title_fullStr |
Assessment of clinical scoring systems for the diagnosis of Williams-Beuren syndrome |
title_full_unstemmed |
Assessment of clinical scoring systems for the diagnosis of Williams-Beuren syndrome |
title_sort |
Assessment of clinical scoring systems for the diagnosis of Williams-Beuren syndrome |
dc.creator.none.fl_str_mv |
Leme, D E S Souza, D H Mercado, Graciela Pastene, E. A. Dias, A Moretti-Ferreira, D |
author |
Leme, D E S |
author_facet |
Leme, D E S Souza, D H Mercado, Graciela Pastene, E. A. Dias, A Moretti-Ferreira, D |
author_role |
author |
author2 |
Souza, D H Mercado, Graciela Pastene, E. A. Dias, A Moretti-Ferreira, D |
author2_role |
author author author author author |
dc.subject.none.fl_str_mv |
Síndrome de Williams Hibridación Fluorescente in Situ Cromosomas Humanos Par 7 |
topic |
Síndrome de Williams Hibridación Fluorescente in Situ Cromosomas Humanos Par 7 |
dc.description.none.fl_txt_mv |
Fil: Leme, D. E. S. Universidade Estadual Paulista. Instituto de Biociencias de Botucatu. Departamento de Genética. Servico de Aconselhamento Genético; Brasil. Fil: Souza, D. H. Universidade Estadual Paulista. Instituto de Biociencias de Botucatu. Departamento de Genética. Servico de Aconselhamento Genético; Brasil. Fil: Mercado, Graciela. ANLIS Dr.C.G.Malbrán. Centro Nacional de Genética Médica; Argentina. Fil: Pastene, E. ANLIS Dr.C.G.Malbrán. Centro Nacional de Genética Médica; Argentina. Fil: Dias, A. Universidade Estadual Paulista. Faculdade de Medicina de Botucatu. Departamento de Saúde Pública; Brasil. Fil: Moretti-Ferreira, D. Universidade Estadual Paulista. Instituto de Biociencias de Botucatu. Departamento de Genética. Servico de Aconselhamento Genético; Brasil. 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. |
description |
Fil: Leme, D. E. S. Universidade Estadual Paulista. Instituto de Biociencias de Botucatu. Departamento de Genética. Servico de Aconselhamento Genético; Brasil. |
publishDate |
2013 |
dc.date.none.fl_str_mv |
2013-09-04 |
dc.type.none.fl_str_mv |
info:ar-repo/semantics/articulo info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.none.fl_str_mv |
https://www.geneticsmr.com/articles/2399 http://sgc.anlis.gob.ar/handle/123456789/1966 https://doi.org/10.4238/2013.September.4.7 |
url |
https://www.geneticsmr.com/articles/2399 http://sgc.anlis.gob.ar/handle/123456789/1966 https://doi.org/10.4238/2013.September.4.7 |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Genetics and molecular research |
dc.rights.none.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.source.none.fl_str_mv |
reponame:Sistema de Gestión del Conocimiento ANLIS MALBRÁN instname:Administración Nacional de Laboratorios e Institutos de Salud "Dr. Carlos G. Malbrán" instacron:ANLIS |
reponame_str |
Sistema de Gestión del Conocimiento ANLIS MALBRÁN |
collection |
Sistema de Gestión del Conocimiento ANLIS MALBRÁN |
instname_str |
Administración Nacional de Laboratorios e Institutos de Salud "Dr. Carlos G. Malbrán" |
instacron_str |
ANLIS |
institution |
ANLIS |
repository.name.fl_str_mv |
Sistema de Gestión del Conocimiento ANLIS MALBRÁN - Administración Nacional de Laboratorios e Institutos de Salud "Dr. Carlos G. Malbrán" |
repository.mail.fl_str_mv |
biblioteca@anlis.gov.ar |
_version_ |
1842344423120175104 |
score |
12.623145 |