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Severe dilative Cardiomyopathy in mucopolysaccharidosis type 1 (Hurler's Syndrome)

S Eichholz, N Lorenz,J Kreuder, T Logeswaran,D Schranz,M Kabus

Neuropediatrics（2008）

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Abstract
Introduction: A dilative cardiomyopathy (DCM) is rarely the first sign in an infant with Mucopolysaccharidosis type 1.
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Mucopolysaccharidoses
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