Dr.RAUNAQ KHANNA, K19608
AIM: To report a rare case of benign familial fleck disorder.
METHOD: This report presents multimodal imaging of a 46-year-old man who presented with dimision of vison in the Right eye since 10 years (visual acuity 6/60 on snellens chart),and posterior segment showing a ONH pallor in the right eye and flecks extending to the post-equatorial region in both eyes hence diagnosed with benign familial fleck retina, an uncommon disorder. Fundus photographs revealed retinal flecks that affected his post-equatorial retina but spared the fovea. Spectral Domain Optical coherence tomography shows intact outer retina and normal macular thickness.
CONCLUSION: Benign familial fleck retina belongs to a heterogenous group of so-called flecked retina syndromes, and should be considered in patients with yellowish-white retinal lesions without involvement of the macula.
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