Central Retinal Artery Occlusion Due to MTHFR A1298C Mutation

Central Retinal Artery Occlusion Due to MTHFR A1298C Mutation

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 A1...

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Veröffentlicht in:Çukurova Üniversitesi tip fakültesi dergisi 2015-09, Vol.40 (3), p.632-635
Hauptverfasser: Turgay Demir, Harun Kara, Filiz Koc, Meltem Demirkiran
Format: Artikel
Sprache:eng ; tur
Schlagworte:
Central retinal artery occlusion
hypercoagulability
MTHFR mutation
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Zusammenfassung: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. [Cukurova Med J 2015; 40(3.000): 632-635]
ISSN:0250-5150