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Figure 2 | Molecular Neurodegeneration

Figure 2

From: Solving a 50 year mystery of a missing OPA1 mutation: more insights from the first family diagnosed with autosomal dominant optic atrophy

Figure 2

Clinical picture of two patients that had been examined already by W. J├Ąger. (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).

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