Chiari malformation type 1 presenting as unilateral progressive foot drop: a case report and review of literature
Author:
Publisher
Springer Science and Business Media LLC
Subject
Pediatrics, Perinatology and Child Health
Link
http://link.springer.com/content/pdf/10.1186/s12887-018-1028-8.pdf
Reference12 articles.
1. Greenberg MS. Chiari Malformation. In: Handbook of Neurosurgery. New york: Thieme; 2006. p. 103–9.
2. Speer MC, George TM, Enterline DS, Franklin A, Wolpert CM, Milhorat TH. A genetic hypothesis for Chiari I malformation with or without syringomyelia. Neurosurg Focus. 2000;8(3):E12.
3. Boyles AL, Enterline DS, Hammock PH, Siegel DG, Slifer SH, Mehltretter L, Gilbert JR, Hu-Lince D, Stephan D, Batzdorf U, et al. Phenotypic definition of Chiari type I malformation coupled with high-density SNP genome screen shows significant evidence for linkage to regions on chromosomes 9 and 15. Am J Med Genet A. 2006;140(24):2776–85.
4. Milhorat TH, Bolognese PA, Nishikawa M, McDonnell NB, Francomano CA. Syndrome of occipitoatlantoaxial hypermobility, cranial settling, and chiari malformation type I in patients with hereditary disorders of connective tissue. J Neurosurg Spine. 2007;7(6):601–9.
5. Tubbs RS, Lyerly MJ, Loukas M, Shoja MM, Oakes WJ. The pediatric Chiari I malformation: a review. Childs Nerv Syst. 2007;23(11):1239–50.
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1. Chiari malformation in a restricted-resource setting and treatment challenges: Case report and literature review;2024-02-12
2. The Role of Neurophysiology in Managing Patients with Chiari Malformations;Journal of Clinical Medicine;2023-10-11
3. Two differential cavities in syringomyelia of pediatric Chiari I malformation presenting with unilateral foot drop;Brain and Development;2023-03
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