Mandibulofacial Syndrome With Growth and Mental Retardation, Microcephaly, Ear Anomalies With Skin Tags, and Cleft Palate in a Mother and Her Son: Autosomal Dominant or X-Linked Syndrome?
Contribuinte(s) |
UNIVERSIDADE DE SÃO PAULO |
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Data(s) |
20/10/2012
20/10/2012
2009
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Resumo |
We report on a Brazilian mother and her son affected with mandibulofacial dysostosis, growth and mental retardation, microcephaly, first branchial arch anomalies, and cleft palate. To date only three males and one female, all sporadic cases, with a similar condition have been reported. This article describes the first familial case with this rare condition indicating autosomal dominant or X-linked inheritance. (C) 2009 Wiley-Liss, Inc. State of Sao Paulo Research Foundation (FAPESP-CEPID) Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) National Council for Scientific and Technological Development (CNPq)[310659/2006-0] |
Identificador |
AMERICAN JOURNAL OF MEDICAL GENETICS PART A, v.149A, n.12, p.2762-2764, 2009 1552-4825 http://producao.usp.br/handle/BDPI/27530 10.1002/ajmg.a.32816 |
Idioma(s) |
eng |
Publicador |
WILEY-LISS |
Relação |
American Journal of Medical Genetics Part A |
Direitos |
restrictedAccess Copyright WILEY-LISS |
Palavras-Chave | #mandibulofacial dysostosis #branchial arch #speech delay #TREACHER-COLLINS-SYNDROME #DYSOSTOSIS #MUTATION #TCOF1 #Genetics & Heredity |
Tipo |
article original article publishedVersion |