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Dandy walker malformation and hypertrophic cardiomyopathy. Unusual fatal association
Neurosciences. 2009; 14 (4): 368-370
in English | IMEMR | ID: emr-136919
ABSTRACT
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
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Index: IMEMR (Eastern Mediterranean) Main subject: Abnormalities, Multiple / Cardiomyopathy, Hypertrophic / Brain / Infant, Newborn / Fatal Outcome Type of study: Case report Limits: Humans / Male Language: English Journal: Neurosciences Year: 2009

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Index: IMEMR (Eastern Mediterranean) Main subject: Abnormalities, Multiple / Cardiomyopathy, Hypertrophic / Brain / Infant, Newborn / Fatal Outcome Type of study: Case report Limits: Humans / Male Language: English Journal: Neurosciences Year: 2009