Sveinsson's chorioretinal atrophy

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Sveinsson's chorioretinal atrophy

An 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.

Molecular pathology
Defects of TEAD1, which encodes a ubiquitous transcription enhancer of the TEA/ATTS domain family, cause Sveinsson's chorioretinal atrophy.
References in periodicals archive ?
Through its flagship SC Launch programme, this SCRA business sector makes investments in and offers support services to South Carolina's early stage, start-up technology companies.
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Servicemembers Civil Relief Act
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by which some of our members have concluded that SCRA is endorsing certain candidates," wrote President Andy Dymond, who did not identify any of the candidates.
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