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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Detalles Bibliográficos
Autores principales: Grant, Nathan, Taylor, J. Michael, Plummer, Zach, Myers, Kasiani, Burrow, Thomas, Luchtman-Jones, Lori, Byars, Anna, Hammill, Adrienne, Wusick, Katie, Smith, Edward, Leach, James, Vadivelu, Sudhakar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Pediatrics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8224401/
https://www.ncbi.nlm.nih.gov/pubmed/34178879
http://dx.doi.org/10.3389/fped.2021.606905

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8224401/
https://www.ncbi.nlm.nih.gov/pubmed/34178879
http://dx.doi.org/10.3389/fped.2021.606905

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