Case Report: Cerebral Revascularization in a Child With Mucopolysaccharidosis Type I

Case Report: Cerebral Revascularization in a Child With Mucopolysaccharidosis Type I

Mucopolysaccharidosis (MPS) type I is a rare lysosomal storage disorder caused by an accumulation of glycosaminoglycans (GAGs) resulting in multisystem disease. Neurological morbidity includes hydrocephalus, spinal cord compression, and cognitive decline. While many neurological symptoms have been d...

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Bibliographic Details
Main Authors: Nathan Grant, J. Michael Taylor, Zach Plummer, Kasiani Myers, Thomas Burrow, Lori Luchtman-Jones, Anna Byars, Adrienne Hammill, Katie Wusick, Edward Smith, James Leach, Sudhakar Vadivelu
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-06-01
Series:Frontiers in Pediatrics
Subjects:
mucopolysaccharidosis I
stroke
cerebral arteriopathy
ventriculomegaly
pial synangiosis
cerebral revascularization
Online Access:https://www.frontiersin.org/articles/10.3389/fped.2021.606905/full

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https://www.frontiersin.org/articles/10.3389/fped.2021.606905/full

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