Management of lateral meningocele syndrome in a child without neurological symptoms and literature review
Author:
Publisher
Springer Science and Business Media LLC
Subject
Neurology (clinical),General Medicine,Pediatrics, Perinatology and Child Health
Link
https://link.springer.com/content/pdf/10.1007/s00381-022-05466-y.pdf
Reference18 articles.
1. Gripp KW, Robbins KM, Sobreira NL et al (2015) Truncating mutations in the last exon of NOTCH3 cause lateral meningocele syndrome. Am J Med Genet A 167A(2):271–281. https://doi.org/10.1002/ajmg.a.36863
2. Ejaz R, Carter M, Gripp K (2016) Lateral meningocele syndrome. In: Adam MP, Ardinger HH, Pagon RA, et al., eds. GeneReviews®. Seattle (WA): University of Washington, Seattle; June 23
3. Brown EC, Gupta K, Sayama C (2017) Neurosurgical management in lateral meningocele syndrome: case report. J Neurosurg Pediatr 19(2):232–238. https://doi.org/10.3171/2016.9.PEDS16311
4. Yamada M, Arimitsu T, Suzuki H, Miwa T, Kosaki K (2021) Early diagnosis of lateral meningocele syndrome in an infant without neurological symptoms based on genomic analysis [published online ahead of print, 2021 Jun 13]. Childs Nerv Syst.https://doi.org/10.1007/s00381-021-05232-6
5. Cuoco JA, Klein BJ, Busch CM et al (2020) Neurosurgical management of lateral meningocele syndrome: a clinical update for the pediatric neurosurgeon. Pediatr Neurosurg 55(1):2–11. https://doi.org/10.1159/000504060
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