Author/Authors
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
Title Of Article
Central Retinal Artery Occlusion Due to MTHFR A1298C Mutation
شماره ركورد
24099
Abstract
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.
From Page
632
NaturalLanguageKeyword
Central retinal artery occlusion , MTHFR mutation , hypercoagulability
JournalTitle
Cukurova Medical Journal
To Page
635
JournalTitle
Cukurova Medical Journal
Link To Document