Neurol. praxi. 2020;21(3):230-234 | DOI: 10.36290/neu.2019.032

Familial cerebral cavernous malformation: clinical case

MUDr. Júlia Travkina, MUDr. Eva Gödöllová, MUDr. Oto Petrík, MPH
Neurologické oddelenie NsP Sv. Lukáša, Galanta

Familial cerebral cavernous malformation is a rare genetically conditioned vascular, affecting predominantly the central nervous system, causing neurological symptomatology, epilepsy, recurrent intracerebral hemorrhages. We would like to present the case of a young female patient, which was diagnosed with familial cerebral cavernous malformation in its rarest genetic form.

Keywords: familial cerebral cavernous malformation, rare vascular anomalies, cephalgias, intracerebral hemorrhages.

Received: April 8, 2019; Accepted: April 25, 2019; Published: June 18, 2020  Show citation

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Travkina J, Gödöllová E, Petrík O. Familial cerebral cavernous malformation: clinical case. Neurol. praxi. 2020;21(3):230-234. doi: 10.36290/neu.2019.032.
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