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?


Autoria(s): GUION-ALMEIDA, Maria Leine; VENDRAMINI-PITTOLI, Siulan; PASSOS-BUENO, Maria Rita Santos; ZECHI-CEIDEI, Roseli Maria
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

20/10/2012

20/10/2012

2009

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

http://dx.doi.org/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