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Saudi Med J ; 23(3): 338-40, 2002 Mar.
Article in English | MEDLINE | ID: mdl-11938430

ABSTRACT

An Omani infant boy who presented in the neonatal period with cardiac failure secondary to hypertrophic cardiomyopathy is reported. He subsequently progressed to show features of a metabolic disorder with multisystem involvement and was diagnosed to have Type II glycogenosis (Pompe's disease). The differential diagnosis and management of metabolic cardiomyopathy are outlined.


Subject(s)
Cardiomyopathy, Hypertrophic/etiology , Glycogen Storage Disease Type II/complications , Cardiomyopathy, Hypertrophic/diagnostic imaging , Fatal Outcome , Glycogen Storage Disease Type II/pathology , Humans , Infant , Male , Ultrasonography
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