Sveinsson's chorioretinal atrophy
Sveinsson's chorioretinal atrophyAn extremely rare autosomal dominant (OMIM:108985) that primarily affects Icelandics, with most cases tracing back to a male founder born in 1540, characterised by symmetrical lesions radiating from the optic disk involving the retina and the choroid.
Defects of TEAD1, which encodes a ubiquitous transcription enhancer of the TEA/ATTS domain family, cause Sveinsson's chorioretinal atrophy.
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