central areolar choroidal dystrophy


Also found in: Acronyms.

central areolar choroidal dystrophy

an autosomal dominant progressive disorder of vision loss with well-demarcated areas of atrophy of retinal pigment epithelium and choriocapillaris.

cen·tral a·re·o·lar chor·oid·al dys·tro·phy

(sen'trăl ă-rē'ŏ-lăr kōr-oyd'ăl dis'trŏ-fē)
An autosomal dominant progressive disorder of vision loss with well-demarcated areas of atrophy of the pigmented layer of the retina and choriocapillaris
References in periodicals archive ?
Posterior polar central choroidal dystrophy affects a larger area than central areolar choroidal dystrophy and in our case the patient was in the advanced stage.
Full-field electroretinograms in patients with central areolar choroidal dystrophy Acta Ophthalmol (Copenh) 1994;72:537-544.
Electrophysiology findings in a large family with central areolar choroidal dystrophy Doc Ophthalmol.
Fine localisation of the gene for central areolar choroidal dystrophy on chromosome 17p.
Autosomal dominant central areolar choroidal dystrophy caused by a mutation in codon 142 in the peripherin/RDS gene.
A point mutation in the RDS-peripherin gene in a Spanish family with central areolar choroidal dystrophy.

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