A neuro-Behçet case with oromandibular dystonia as the first sign
Behçet’s disease is a chronic, multisystemic, inflammatory, recurrent vasculitis that clinically presents with oral aphthae, genital ulcer, skin lesions, and ophthalmologic findings. The involvement of this disease in the central nervous system is known as neuro-Behçet syndrome. Herein, we presented a rare case of neuro-Behçet in a 45-year-old female patient presenting with oromandibular dystonia, discussed in light of the literature.
Authors
- Nazlı Gamze Bülbül (ORCID: https://orcid.org/0000-0001-8560-0774)
Institutions
- İstanbul Eğitim ve Araştırma Hastanesi (TR)
Publication Details
- Journal
- Journal of Parkinson’s Disease and Movement Disorders
- Published
- 2025-08-13
- DOI
- https://doi.org/10.5606/phhb.dergisi.2023.19
- Primary Topic
- Ocular Diseases and Behçet’s Syndrome
- Type
- article
- Field-Weighted Citation Impact
- 0.00