Longitudinal clinical and imaging analysis of hydrocephalus in a single-center study in 57 patients with mucopolysaccharidosis type IH (Hurler syndrome)

In patients without preexisting hydrocephalus, no new cases of hydrocephalus developed, and ventricular size stabilized within 2 years after transplant. The authors call into question the overall utility of serial brain MRI after transplant in patients with MPS IH.

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Publication Details

Journal
Journal of Neurosurgery Pediatrics
Published
2025-05-09
DOI
https://doi.org/10.3171/2025.2.peds24476
Primary Topic
Cerebrospinal fluid and hydrocephalus
Type
article
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article

Longitudinal clinical and imaging analysis of hydrocephalus in a single-center study in 57 patients with mucopolysaccharidosis type IH (Hurler syndrome)

Carolina Sandoval-Garcia, Shiwei Huang, Julie B. Eisengart, David Nascene et al.
Journal of Neurosurgery Pediatrics
Cerebrospinal fluid and hydrocephalus
article

Longitudinal clinical and imaging analysis of hydrocephalus in a single-center study in 57 patients with mucopolysaccharidosis type IH (Hurler syndrome)

Carolina Sandoval-Garcia, Shiwei Huang, Julie B. Eisengart, David Nascene, Troy C. Lund, Paul J. Orchard, Ashish O. Gupta, Ryan Shanley, Moo‐Yeol Choi, Daniel Guillaume
article en

Abstract

In patients without preexisting hydrocephalus, no new cases of hydrocephalus developed, and ventricular size stabilized within 2 years after transplant. The authors call into question the overall utility of serial brain MRI after transplant in patients with MPS IH.

Journal of Neurosurgery PediatricsVol. 36(2)
University of Minnesota (US), University Radiology (US)
Good health and well-being
Openalex Percentile: Top 89%
Cerebrospinal fluid and hydrocephalus
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