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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Detalles Bibliográficos
Autores principales: Machnikowska-Sokołowska, Magdalena, Myszczuk, Aleksandra, Wieszała, Emilia, Wieja-Błach, Dominika, Jamroz, Ewa, Paprocka, Justyna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9962124/
https://www.ncbi.nlm.nih.gov/pubmed/36837830
http://dx.doi.org/10.3390/metabo13020209

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9962124/
https://www.ncbi.nlm.nih.gov/pubmed/36837830
http://dx.doi.org/10.3390/metabo13020209

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