Intellectual disability, unusual facial morphology and hand anomalies in sibs

Detalhes bibliográficos
Autor(a) principal: Sousa, SB
Data de Publicação: 2013
Outros Autores: Venâncio, M, Chanudet, E, Palmer, R, Ramos, L, Beales, PL, Moore, GE, Saraiva, JM, Hennekam, RC
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10400.4/1589
Resumo: Here we report on a Portuguese family with three sisters who shared moderate intellectual disability, unusual facial morphology (short palpebral fissures; broad nasal tip; thin upper and lower vermillion; broad and pointed chin) and hand anomalies in two of them (short left third and fifth right metacarpals in one case; marked syndactyly between the third and fourth fingers in another). One of the sisters had microcephaly and short stature, and the other two were obese. Obesity and somewhat similar facial features were also present in the otherwise healthy mother. Despite the overlap with several known syndromes (Albright osteodystrophy; Filippi syndrome; Rubinstein-Taybi syndrome; microdeletion 2q37), we suggest this condition is previously unreported, and most likely displays an autosomal recessive pattern of inheritance.
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spelling Intellectual disability, unusual facial morphology and hand anomalies in sibsDeficiência IntelectualAnomalias Congénitas MúltiplasFaciesMãoHere we report on a Portuguese family with three sisters who shared moderate intellectual disability, unusual facial morphology (short palpebral fissures; broad nasal tip; thin upper and lower vermillion; broad and pointed chin) and hand anomalies in two of them (short left third and fifth right metacarpals in one case; marked syndactyly between the third and fourth fingers in another). One of the sisters had microcephaly and short stature, and the other two were obese. Obesity and somewhat similar facial features were also present in the otherwise healthy mother. Despite the overlap with several known syndromes (Albright osteodystrophy; Filippi syndrome; Rubinstein-Taybi syndrome; microdeletion 2q37), we suggest this condition is previously unreported, and most likely displays an autosomal recessive pattern of inheritance.WileyRIHUCSousa, SBVenâncio, MChanudet, EPalmer, RRamos, LBeales, PLMoore, GESaraiva, JMHennekam, RC2013-11-06T10:45:14Z20132013-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.4/1589engAm J Med Genet A. 2013;161(10):2401-6.info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-07-11T14:22:51Zoai:rihuc.huc.min-saude.pt:10400.4/1589Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T18:04:04.738772Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Intellectual disability, unusual facial morphology and hand anomalies in sibs
title Intellectual disability, unusual facial morphology and hand anomalies in sibs
spellingShingle Intellectual disability, unusual facial morphology and hand anomalies in sibs
Sousa, SB
Deficiência Intelectual
Anomalias Congénitas Múltiplas
Facies
Mão
title_short Intellectual disability, unusual facial morphology and hand anomalies in sibs
title_full Intellectual disability, unusual facial morphology and hand anomalies in sibs
title_fullStr Intellectual disability, unusual facial morphology and hand anomalies in sibs
title_full_unstemmed Intellectual disability, unusual facial morphology and hand anomalies in sibs
title_sort Intellectual disability, unusual facial morphology and hand anomalies in sibs
author Sousa, SB
author_facet Sousa, SB
Venâncio, M
Chanudet, E
Palmer, R
Ramos, L
Beales, PL
Moore, GE
Saraiva, JM
Hennekam, RC
author_role author
author2 Venâncio, M
Chanudet, E
Palmer, R
Ramos, L
Beales, PL
Moore, GE
Saraiva, JM
Hennekam, RC
author2_role author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv RIHUC
dc.contributor.author.fl_str_mv Sousa, SB
Venâncio, M
Chanudet, E
Palmer, R
Ramos, L
Beales, PL
Moore, GE
Saraiva, JM
Hennekam, RC
dc.subject.por.fl_str_mv Deficiência Intelectual
Anomalias Congénitas Múltiplas
Facies
Mão
topic Deficiência Intelectual
Anomalias Congénitas Múltiplas
Facies
Mão
description Here we report on a Portuguese family with three sisters who shared moderate intellectual disability, unusual facial morphology (short palpebral fissures; broad nasal tip; thin upper and lower vermillion; broad and pointed chin) and hand anomalies in two of them (short left third and fifth right metacarpals in one case; marked syndactyly between the third and fourth fingers in another). One of the sisters had microcephaly and short stature, and the other two were obese. Obesity and somewhat similar facial features were also present in the otherwise healthy mother. Despite the overlap with several known syndromes (Albright osteodystrophy; Filippi syndrome; Rubinstein-Taybi syndrome; microdeletion 2q37), we suggest this condition is previously unreported, and most likely displays an autosomal recessive pattern of inheritance.
publishDate 2013
dc.date.none.fl_str_mv 2013-11-06T10:45:14Z
2013
2013-01-01T00:00:00Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
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dc.identifier.uri.fl_str_mv http://hdl.handle.net/10400.4/1589
url http://hdl.handle.net/10400.4/1589
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Am J Med Genet A. 2013;161(10):2401-6.
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dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Wiley
publisher.none.fl_str_mv Wiley
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collection Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
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