Doyne honeycomb retinal dystrophy

A retinal drusen characterized by yellow-white deposits (drusen) that accumulate beneath the retinal pigment epithelium in the posterior pole of the eye in a honeycomb pattern and that has_material_basis_in mutations in the EFEMP1 gene on chromosome 2p16.

Signs and symptoms

• Reticular pigmentary degeneration
• Visual impairment
• Retinal dystrophy

Also known as: DHRD; Doyne honeycomb degeneration of retina