Possible New Syndrome: Left Ventricular Noncompaction, Partial Agenesis of the Corpus Callosum, and Developmental Delay in a Brazilian Child

dc.contributorUniversidade de São Paulo (USP)
dc.contributorUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2014-05-20T13:31:32Z
dc.date.accessioned2022-10-05T13:35:23Z
dc.date.available2014-05-20T13:31:32Z
dc.date.available2022-10-05T13:35:23Z
dc.date.created2014-05-20T13:31:32Z
dc.date.issued2009-05-01
dc.identifierAmerican Journal of Medical Genetics Part A. Hoboken: Wiley-liss, v. 149A, n. 5, p. 1041-1045, 2009.
dc.identifier1552-4825
dc.identifierhttp://hdl.handle.net/11449/10739
dc.identifier10.1002/ajmg.a.32787
dc.identifierWOS:000265805900035
dc.identifier2331180822532901
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/3886829
dc.description.abstractWe 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.
dc.languageeng
dc.publisherWiley-liss
dc.relationAmerican Journal of Medical Genetics Part A
dc.relation2.264
dc.relation1,098
dc.rightsAcesso restrito
dc.sourceWeb of Science
dc.subjectleft ventricular noncompaction cardiomyopathy
dc.subjectmental retardation
dc.subjectspeech/language disorders
dc.titlePossible New Syndrome: Left Ventricular Noncompaction, Partial Agenesis of the Corpus Callosum, and Developmental Delay in a Brazilian Child
dc.typeArtigo


Este ítem pertenece a la siguiente institución