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Intellectual disability, unusual facial morphology and hand anomalies in sibs

Bibliographic Details
Main Author: Sousa, SB
Publication Date: 2013
Other Authors: Venâncio, M, Chanudet, E, Palmer, R, Ramos, L, Beales, PL, Moore, GE, Saraiva, JM, Hennekam, RC
Format: Article
Language: eng
Source: Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
Download full: http://hdl.handle.net/10400.4/1589
Summary: 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/10400.4/1589enginfo:eu-repo/semantics/openAccessreponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiainstacron:RCAAP2025-01-30T03:21:21Zoai:rihuc.huc.min-saude.pt:10400.4/1589Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireinfo@rcaap.ptopendoar:https://opendoar.ac.uk/repository/71602025-05-28T19:44:06.000369Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiafalse
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
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