A case of adult-onset Sturge-Weber syndrome type III without intracranial calcification, presenting with transient homonymous hemianopia
Author:
Affiliation:
1. Department of Neurology, Toyonaka Municipal Hospital
Publisher
Societas Neurologica Japonica
Subject
Neurology (clinical)
Link
https://www.jstage.jst.go.jp/article/clinicalneurol/61/2/61_cn-001473/_pdf
Reference9 articles.
1. 1) Cho S, Maharathi B, Ball KL, et al. Sturge-Weber syndrome patient registry: delayed diagnosis and poor seizure control. J Pediatr 2019;215:158-163.
2. 3) Siri L, Giordano L, Accorci P, et al. Clinical features of Sturge-Weber syndrome without facial nevus: five novel cases. Eur J Paediatr Neurol 2013;17:91-96.
3. 4) Klapper J. Headache in Sturge-Weber syndrome. Headache 1994;34:521-522.
4. 5) Comi A. Current therapeutic options in Sturge-Weber synrdome. Semin pediatr neurol 2015;22:295-301.
5. 6) Wyllie E, Gupta A, Lachhwani DK. The treatment of epilepsy, principles & practice. 4th ed. Philadelphia: Lippincott Williams & Wilkins; 2005. p. 540.
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