2023
DOI: 10.1017/s1047951123003347
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Natural history of cardiac findings in mucopolysaccharidosis type I: report from an international registry

Elizabeth Braunlin,
Luisa Bay,
Nathalie Guffon
et al.

Abstract: Mucopolysaccharidosis type I is an inborn error of glycosaminoglycan catabolism with phenotypes ranging from severe (Hurler syndrome) to attenuated (Hurler–Scheie and Scheie syndromes). Cardiovascular involvement is common and contributes significantly to morbidity and mortality. We conducted a retrospective analysis of the prevalence and natural history of cardiac abnormalities in treatment-naïve individuals enrolled in the international Mucopolysaccharidosis Type I Registry. Interrogation of echocardiography… Show more

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