Intellectual disability, unusual facial morphology and hand anomalies in sibs
Main Author: | |
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Publication Date: | 2013 |
Other Authors: | , , , , , , , |
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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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 |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://hdl.handle.net/10400.4/1589 |
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http://hdl.handle.net/10400.4/1589 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
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info:eu-repo/semantics/openAccess |
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openAccess |
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application/pdf |
dc.publisher.none.fl_str_mv |
Wiley |
publisher.none.fl_str_mv |
Wiley |
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