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

• Main Authors: Nathan Grant (Author), J. Michael Taylor (Author), Zach Plummer (Author), Kasiani Myers (Author), Thomas Burrow (Author), Lori Luchtman-Jones (Author), Anna Byars (Author), Adrienne Hammill (Author), Katie Wusick (Author), Edward Smith (Author), James Leach (Author), Sudhakar Vadivelu (Author)
• Format: Book
• Published: Frontiers Media S.A., 2021-06-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.

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...