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Neurosciences. 2009; 14 (4): 368-370
em Inglês | IMEMR | ID: emr-136919

RESUMO

Dandy Walker malformation [DWM] is a rare congenital brain anomaly characterized by cystic dilation of the fourth ventricle and hypoplasia of the cerebellar vermis. Other extracranial anomalies can be associated, including cardiac defects. We report a rare patient with DWM associated with progressive heart failure secondary to hypertrophic cardiomyopathy. He was diagnosed at 2 months of age and died 5 months later. We conclude that hypertrophic cardiomyopathy can be associated with DWM with poor prognosis. A careful cardiac evaluation is needed in all infants with DWM for early recognition of such potentially serious associated cardiac malformations


Assuntos
Humanos , Masculino , Encéfalo/anormalidades , Cardiomiopatia Hipertrófica/mortalidade , Anormalidades Múltiplas/patologia , Evolução Fatal , Recém-Nascido
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