Fig. 3 | Scientific Reports

Fig. 3

From: Identification of new families and variants in autosomal dominant macular dystrophy associated with THRB

Fig. 3

Electrophysiologic testing performed at patients carrying THRB variants in our IRD-cohort. (A) Electrophysiology testing of patient IV:2-Family 1, compatible with symmetric, bilateral, severe maculopathy. (B) Electrophysiology testing of patient II:4-Family 2, suggestive of macular dysfunction. (C) Electrophysiology testing of patient IV:1-Family 3, compatible with bilateral maculopathy. (D) Electrophysiology testing of patient III:7-Family 3, compatible with bilateral maculopathy, in line with the patient´s symptoms of dyschromatopsia and visual acuity loss. (E) FF-ERG of patient V:3-Family showing responses well within normal limits. However, P-ERG is lacking to correctly assess macular dysfunction.

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