Otro
Possible New Syndrome: Left Ventricular Noncompaction, Partial Agenesis of the Corpus Callosum, and Developmental Delay in a Brazilian Child
Registro en:
American Journal of Medical Genetics Part A. Hoboken: Wiley-liss, v. 149A, n. 5, p. 1041-1045, 2009.
1552-4825
10.1002/ajmg.a.32787
WOS:000265805900035
Autor
Lamonica, Dionisia A. C.
Abramides, Dagma Venturini Marques
Maximino, Luciana P.
Gejao, Mariana G.
da Silva, Greyce K.
Ferreira, Amanda T.
Furlan, Renata H.
Giacheti, Célia Maria
Barros-Neto, Plinio A.
Richieri-Costa, A.
Resumen
We report oil the clinical, neuropsychological and language characteristics of it boy with left ventricular noncompaction cardiomyopathy (LVNC), agenesis of the splenium of the corpus callosum, minor anomalies of face and limbs, mild mental retardation, and speech and language disabilities. The occurrence of pilomatricoma (calcifying epithelioma) may be part of the clinical spectrum or a fortuitous finding. Compared to other related conditions with LVNC suggests that this is a new unique pattern MCA/MR syndrome. (C) 2009 Wiley-Liss, Inc. Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)