Chiari I malformation and syringomyelia in mucopolysaccharidosis type I (Hurler syndrome) treated with posterior fossa decompression: Case report and review of the literature

BACKGROUND: Hurler Syndrome is the most severe phenotype of mucopolysaccharidosis type I. With bone marrow transplant and enzyme replacement therapy, the life expectancy of a child with Hurler syndrome has been extended, predisposing them to multiple musculoskeletal issues most commonly involving th...

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Detalles Bibliográficos
Autores principales: Makler, Vyacheslav, Goldstein, Christina L., Hoernschemeyer, Daniel, Tanaka, Tomoko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2017
Materias:
Pediatric Neurosurgery: Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5461569/
https://www.ncbi.nlm.nih.gov/pubmed/28607814
http://dx.doi.org/10.4103/sni.sni_463_16

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5461569/
https://www.ncbi.nlm.nih.gov/pubmed/28607814
http://dx.doi.org/10.4103/sni.sni_463_16

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