Moyamoya Disease: Clinical and Radiological Characteristics in Adult Greek Patients.
Sofia VassilopoulouArgyro TountopoulouEleni KorompokiGeorgios PapageorgiouDimitrios S KasselimisGeorgios VelonakisAchilles ChatziioannouConstantin PotagasKonstantinos SpengosPublished in: Journal of clinical medicine (2023)
Our MMD patients had a later onset of the disease and an absence of familial occurrence. The most common manifestation was ischemia, transient or permanent, and all lesions affected the anterior circulation, whereas no vascular malformations (AVM, aneurysms) were demonstrated in brain imaging. These findings in Greek patients imply a probable different, Mediterranean phenotype.