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Article

Assessment of the phenotypic range seen in Doyne honeycomb retinal dystrophy.

Archives of ophthalmology (Chicago, Ill. : 1960) - 1 Jul 1997

Evans K, Gregory C Y, Wijesuriya S D, Kermani S, Jay M R, Plant C, Bird A C

Abstract excerpt

OBJECTIVE: Using molecular genetics as the basis for diagnosis, to assess the phenotype in the family originally described as having dominantly inherited Doyne honeycomb retinal dystrophy (DHRD) linked to chromosome 2p16. DESIGN: Clinical examination including fluorescein angiography was undertaken in 107 family members. Nine affected patients underwent electroretinography, perimetry, dark adaptometry,...

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Identifiers

PMID: 9230832
DOI: 10.1001/archopht.1997.01100160074012

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

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