Neurodevelopmental Trajectories in Children with Mucopolysaccharidoses: Clinical Assessment Strategies and Imaging Correlates
DOI:
https://doi.org/10.48047/wthg7h20Keywords:
Neurodevelopmental, Mucopolysaccharidoses, Clinical Assessment , Imaging CorrelatesAbstract
Background: Mucopolysaccharidoses (MPS) represent a heterogeneous group of lysosomal storage disorders characterized by the
accumulation of glycosaminoglycans (GAGs), leading to progressive multisystem involvement and, in several subtypes, significant central nervous system (CNS) pathology.
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References
Neufeld EF, Muenzer J. The mucopolysaccharidoses. In: Valle D, Beaudet AL, Vogelstein B, et al., eds. The Online Metabolic and Molecular Bases of Inherited Disease. McGraw-Hill; 2001.
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