Orofacial abnormalities in mucopolysaccharidosis and mucolipidosis type <scp>II</scp> and <scp>III</scp> : A systematic review-Reference-Cited by-同舟云学术

Orofacial abnormalities in mucopolysaccharidosis and mucolipidosis type II and III : A systematic review

Published:2022-09-21 Issue:6 Volume:63 Page:621-629
ISSN:2192-8312
Container-title:JIMD Reports
language:en
Short-container-title:JIMD Reports

Author:

de Bode Chiel J.¹^ORCID,Dogterom Emma J.²,Rozeboom Antoinette V. J.¹,Langendonk Janneke J.³,Wolvius Eppo B.¹,van der Ploeg Ans T.²,Oussoren Esmée²,Wagenmakers Margreet A. E. M.³^ORCID

Affiliation:

1. Department of Oral & Maxillofacial Surgery Erasmus MC University Medical Center Rotterdam The Netherlands

2. Department of Pediatrics, Center for Lysosomal and Metabolic Diseases, Erasmus MC University Medical Center Rotterdam Rotterdam The Netherlands

3. Department of Internal Medicine, Center for Lysosomal and Metabolic Diseases, Erasmus MC University Medical Center Rotterdam Rotterdam The Netherlands

Publisher

Wiley

Subject

Biochemistry, Genetics and Molecular Biology (miscellaneous),Endocrinology, Diabetes and Metabolism,Internal Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/jmd2.12331

Reference52 articles.

1. The mucopolysaccharidoses: a clinical review and guide to management.

2. Radiological and clinical characterization of the lysosomal storage disorders: non-lipid disorders

3. Bone, joint and tooth development in mucopolysaccharidoses: Relevance to therapeutic options

4. Molecular order in mucolipidosis II and III nomenclature

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