Author/Authors :
Peköz, Taylan Adana Numune Eğitim ve Araştırma Hastanesi - Nöroloji Bölümü, Turkey , Boz, Pınar Bengi Adana Numune Eğitim - Araştırma Hastanesi Nöroloji Bölümü, Turkey , Koç, Filiz Çukurova Üniversitesi - Nöroloji Anabilim Dalı, Turkey
Abstract :
Leber s hereditary optic neuropathy characterized by loss of central vision is often seen in men and a maternally inherited disease. Here, admitted to our clinic with complaints of unilateral visual loss was diagnosed as Leber s hereditary optic neuropathy which was confirmed by the presence of a mutation at 3460G A position.
NaturalLanguageKeyword :
Optic neuropathy , vision loss , inherited , mutation
