Familial Cerebral Cavernous Malformations : A Clinical Series and Literature Review
Advances in molecular genetic testing have allowed for prompt diagnosis and timely management of patients with FCCMs. Surgical treatment is an effective option in symptomatic cases with progressive neurological deficits and refractory epilepsy. Regular neurological monitoring and radiological assessment are recommended in symptomatic cases and asymptomatic carriers.
Authors
- Ali Osman Muçuoğlu (ORCID: https://orcid.org/0000-0003-1748-6337)
- Hüseyin Doğu (ORCID: https://orcid.org/0000-0002-7754-4984)
- Röya Gasımlı (ORCID: https://orcid.org/0000-0002-6760-8921)
- Abdülkerim Gökoğlu (ORCID: https://orcid.org/0000-0001-8071-4078)
- Emre Tepeli (ORCID: https://orcid.org/0000-0003-3771-2741)
- Hidayet Akdemir (ORCID: https://orcid.org/0000-0002-9390-7730)
Institutions
- Ege University (TR)
- Istanbul University (TR)
- Erciyes University (TR)
Publication Details
- Journal
- Journal of Korean Neurosurgical Society
- Published
- 2025-08-28
- DOI
- https://doi.org/10.3340/jkns.2025.0074
- Primary Topic
- Vascular Malformations Diagnosis and Treatment
- Type
- article
- Field-Weighted Citation Impact
- 0.00