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Öğe CADASIL: clinic and genetic corelation(Eskişehir Osmangazi Üniversitesi Rektörlüğü, 2021) Demir, Turgay; İşcan, Dilek; Koç, Filiz; Bisgin, AtılCADASIL (Cerebral Autosomal Dominant Arteriopathy, Subcortical Infarcts, Leukoencephalopathy). It is an autosomal dominant familial small vessel disease caused by the mutation of the Notch3 gene in the short arm of the chromosome 19. Clinically it is characterized by recurrent stroke attacks, migraine or migraineous headaches, epileptic seizures and progressive cognitive impairment. In this article, we report four cases of CADASIL that we have clinically evaluated CADASIL and confirmed the diagnosis by moleculer analyses.
