Sveinsson chorioretinal atrophy

An eye disease characterized by presence in the fundus of progressive bilateral retinal and choroidal atrophy leading to central vision loss that has_material_basis_in heterozygous mutation in TEAD1 on 11p15.3.

Signs and symptoms

• Astigmatism
• Peripapillary chorioretinal atrophy
• Myopia

Also known as: HPCD; SCRA; atrophia areata; helicoid peripapillary chorioretinal degeneration; peripapillary chorioretinal degeneration, Icelandic type