Central Retinal Artery Occlusion Due to MTHFR A1298C Mutation


Demir T. , KARA H., Koc F. , Demirkiran M.

CUKUROVA MEDICAL JOURNAL, cilt.40, ss.632-635, 2015 (ESCI İndekslerine Giren Dergi) identifier

  • Cilt numarası: 40 Konu: 3
  • Basım Tarihi: 2015
  • Dergi Adı: CUKUROVA MEDICAL JOURNAL
  • Sayfa Sayıları: ss.632-635

Özet

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.