Mucopolysaccharidosis Type 1 among Children—Neuroradiological Perspective Based on Single Centre Experience and Literature Review

Mucopolysaccharidosis Type 1 among Children—Neuroradiological Perspective Based on Single Centre Experience and Literature Review

Mucopolysaccharidosis 1 (MPS 1) is a group of rare lysosomal genetic disorders resulting from the accumulation of undegraded glycosaminoglycans (GAGs) leading to multiorgan damage. Neurological symptoms vary from mild to severe. Neuroimaging—mainly magnetic resonance (MRI)—plays a crucial role in di...

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Bibliographic Details
Main Authors: Magdalena Machnikowska-Sokołowska, Aleksandra Myszczuk, Emilia Wieszała, Dominika Wieja-Błach, Ewa Jamroz, Justyna Paprocka
Format: Article
Language:English
Published: MDPI AG 2023-01-01
Series:Metabolites
Subjects:
MPS 1
neuroradiology
mucopolysaccharidosis 1
Hurler disease
GAGs
glycosaminoglycans
Online Access:https://www.mdpi.com/2218-1989/13/2/209

Internet

https://www.mdpi.com/2218-1989/13/2/209

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