Dysostosis in mucopolysaccharidosis type 2: A case of longitudinal follow up and literature review
Abstract
Mucopolysaccharidosis type 2 is a congenital lysosomal disease characterized by iduronate-2-sulfatase deficiency, which leads to excessive accumulation of glycosaminoglycans in tissue. Dysostosis, which primarily involves decreased bone mineralization with morphological changes in the bone, is a major skeletal condition in mucopolysaccharidosis, but its pathophysiology is not well known. Here, we report a case of mucopolysaccharidosis type 2...
Paper Details
Title
Dysostosis in mucopolysaccharidosis type 2: A case of longitudinal follow up and literature review
Published Date
Mar 1, 2021
Journal
Volume
16
Issue
3
Pages
656 - 660
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