Possible new syndrome: Left ventricular noncompaction, partial agenesis of the corpus callosum, and developmental delay in a Brazilian child

We report on the clinical, neuropsychological and language characteristics of a 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 occurr...

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Veröffentlicht in:American journal of medical genetics. Part A 2009-05, Vol.149A (5), p.1041-1045
Hauptverfasser: Lamonica, Dionisia A.C., Abramides, Dagma V.M., Maximino, Luciana P., Gejão, Mariana G., da Silva, Greyce K., Ferreira, Amanda T., Furlan, Renata H., Giacheti, Célia M., Barros‐Neto, Plínio A., Richieri‐Costa, A.
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Sprache:eng
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Zusammenfassung:We report on the clinical, neuropsychological and language characteristics of a 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. © 2009 Wiley‐Liss, Inc.
ISSN:1552-4825
1552-4833
DOI:10.1002/ajmg.a.32787