Figure 2From: Solving a 50 year mystery of a missing OPA1 mutation: more insights from the first family diagnosed with autosomal dominant optic atrophyClinical picture of two patients that had been examined already by W. Jäger. (A) Funduscopy of patient B (V-26) showed pallor of the optic disc with temporal prominence. (B) Visual field of patient A (V-24) showed a clear central scotoma. (C) Patient B showed a decentered central scotoma (excentric retinal locus of fixation, note conjugate displacement of the blind spot).Back to article page