| Literature DB >> 26745646 |
Jennifer Liang1, Ash Singhal1.
Abstract
Hurler syndrome is the most severe form of mucopolysaccharidosis (MPS) Type 1. Progressive neurocognitive decline in this condition can be accompanied by macrocephaly, ventriculomegaly, and/or periventricular signal changes on MRI, which often leads to a neurosurgical referral. In this case, the authors describe a 2-year-old boy with ventriculomegaly and periventricular T2 signal changes, both of which decreased following medical management of Hurler syndrome. The authors discuss the possible mechanisms for this finding and the implications for neurosurgical treatment of this condition.Entities:
Keywords: ERT = enzyme replacement therapy; GAG = glycosaminoglycan; HSCT = hematopoietic stem cell transplant; Hurler syndrome; MPS = mucopolysaccharidosis; congenital; mucopolysaccharidosis Type 1; pediatric neurosurgery; ventriculomegaly
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Year: 2016 PMID: 26745646 DOI: 10.3171/2015.9.PEDS15477
Source DB: PubMed Journal: J Neurosurg Pediatr ISSN: 1933-0707 Impact factor: 2.375