Frontonasal Dysplasia, Severe Neuropsychological Delay, and Midline Central Nervous System Anomalies: Report of 10 Brazilian Male Patients


Autoria(s): GUION-ALMEIDA, Maria Leine; RICHIERI-COSTA, Antonio
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

19/10/2012

19/10/2012

2009

Resumo

Here we report on 10 male patients with frontonasal dysplasia, cleft lip/palate, mental retardation, lack of language acquisition, and severe central nervous system involvement. Imaging studies disclosed absence of the corpus callosum, midline cysts, and an abnormally modeled cerebellum. Neuronal heterotopias were present in five patients and parieto-occipital encephalocele in three patients. We suggest that this pattern found exclusively in males, most likely represents a newly recognized syndrome distilled from the group of disorders subsumed under frontonasal dysplasia. (C) 2009 Wiley-Liss, Inc.

CNPq[310659/2006-0]

Identificador

AMERICAN JOURNAL OF MEDICAL GENETICS PART A, v.149A, n.5, p.1006-1011, 2009

1552-4825

http://producao.usp.br/handle/BDPI/26925

10.1002/ajmg.a.32717

http://dx.doi.org/10.1002/ajmg.a.32717

Idioma(s)

eng

Publicador

WILEY-LISS

Relação

American Journal of Medical Genetics Part A

Direitos

restrictedAccess

Copyright WILEY-LISS

Palavras-Chave #frontal and nasal abnormalities #mental retardation #CNS anomalies #agenesis of the corpus callosum #CLEFT FACE SYNDROME #MENTAL-RETARDATION #MEDIAN CLEFT #CRANIOFRONTONASAL SYNDROME #DIFFERENTIAL-DIAGNOSIS #NASAL DYSOSTOSIS #MALFORMATION #LIP #HYPERTELORISM #PALATE #Genetics & Heredity
Tipo

article

original article

publishedVersion