Imaging hallmarks of mucopolysaccharidosis in a young Ethiopian boy: A case report

Imaging hallmarks of mucopolysaccharidosis in a young Ethiopian boy: A case report

Mucopolysaccharidoses (MPS) are lysosomal storage disorders resulting from deficiencies in specific enzymes (lysosomal hydrolases), leading to the accumulation of excessive mucopolysaccharides (glycosaminoglycan’s, GAGs). These conditions are typically inherited in an autosomal recessive pattern, ex...

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Bibliographic Details
Main Authors: Muluken Yifru Gebresilassie, MD, Abdudin Heru Mehammed, MD, Misganaw Yigletie Damtie, MD, Hawi Dida Midekso, MD, Natnael Alemu Bezabih, MD, Michael Teklehaimanot Abera, MD, Atsede Birhanu Worku, MD
Format: Article
Language:English
Published: Elsevier 2025-09-01
Series:Radiology Case Reports
Subjects:
Mucopolysaccharidosis
Hurler syndrome
Hunter syndrome
Morquio syndrome
Ethiopia
Online Access:http://www.sciencedirect.com/science/article/pii/S193004332500545X
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