Cardiovascular manifestations of mucopolysaccharidosis type VI (Maroteaux–Lamy syndrome)

Author:

Golda Adam,Jurecka Agnieszka,Tylki-Szymanska Anna

Publisher

Elsevier BV

Subject

Cardiology and Cardiovascular Medicine

Reference44 articles.

1. Cumulative incidence rates of the mucopolysaccharidoses in Germany;Baehner;J Inherit Metab Dis,2005

2. Mucopolysaccharidoses in the Scandinavian countries: incidence and prevalence;Malm;Acta Paediatr,2008

3. The mucopolysaccharidoses;Neufeld,2001

4. Mucopolysaccharidosis VI;Valayannopoulos;Orphanet J Rare Dis,2010

5. Mitral and aortic regurgitation in 84 patients with mucopolysaccharidoses;Wippermann;Eur J Pediatr,1995

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1. Evaluation of cardiac findings in mucopolysaccharidosis;The International Journal of Cardiovascular Imaging;2023-10-17

2. Metabolic Cardiomyopathies and Cardiac Defects in Inherited Disorders of Carbohydrate Metabolism: A Systematic Review;International Journal of Molecular Sciences;2023-05-11

3. Pre-operative Considerations in Adult Mucopolysaccharidosis Patients Planned for Cardiac Intervention;Frontiers in Cardiovascular Medicine;2022-04-04

4. Mucopolysaccharidoses;Emery and Rimoin's Principles and Practice of Medical Genetics and Genomics;2021

5. A case of mucopolysaccharidosis type VI in a polish family. Importance of genetic testing and genotype-phenotype relationship in the diagnosis of mucopolysaccharidosis;Molecular Genetics and Metabolism Reports;2020-12

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