Dysostosis in mucopolysaccharidosis type 2: A case of longitudinal follow up and literature review

Dysostosis in mucopolysaccharidosis type 2: A case of longitudinal follow up and literature review

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 maj...

Full description

Bibliographic Details
Main Authors: Tomoaki Sasaki, MD, PhD, Miki Ogata, MD, Aya Kajihama, MD, Kouichi Nakau, MD, Atsutaka Okizaki, MD, PhD
Format: Article
Language:English
Published: Elsevier 2021-03-01
Series:Radiology Case Reports
Subjects:
Mucopolysaccharidosis type 2
Dysostosis
Cranial hyperostosis
Online Access:http://www.sciencedirect.com/science/article/pii/S1930043321000030

Internet

http://www.sciencedirect.com/science/article/pii/S1930043321000030

Similar Items