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Neurológia pre prax 3/2020
Familial cerebral cavernous malformation: clinical case
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
