Demir, Turgay Çukurova Üniversitesi - Tıp Fakültesi - Nöroloji Anabilim Dalı, Turkey , Kara, Harun Çukurova Üniversitesi - Tıp Fakültesi - Nöroloji Anabilim Dalı, Turkey , Koç, Filiz Çukurova Üniversitesi - Tıp Fakültesi - Nöroloji Anabilim Dalı, Turkey , Demirkıran, Meltem Çukurova Üniversitesi - Tıp Fakültesi - Nöroloji Anabilim Dalı, Turkey

Central Retinal Artery Occlusion Due to MTHFR A1298C Mutation

24099

Central retinal artery occlusion (CRAO), a rare condition, is an important cause of acute vision loss. It always seen in elderly. CRAO is observed in youngs , if the patient has hypercoagulability. Here we presented a case who developed neurological findings due to CRAO with the mutation of MTHFR A1298C.

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Central retinal artery occlusion , MTHFR mutation , hypercoagulability

Cukurova Medical Journal

635