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Article

Structural disease progression in PDE6-associated autosomal recessive retinitis pigmentosa.

Ophthalmic genetics - 1 Oct 2018

Takahashi Vitor K L, Takiuti Júlia T, Jauregui Ruben, Lima Luiz H, Tsang Stephen H

Abstract excerpt

BACKGROUND AND OBJECTIVE: To evaluate the progression of retinitis pigmentosa (RP) caused by mutations in either PDE6A or PDE6B by measuring the progressive constriction of the hyperautofluorescent ring and shortening of the ellipsoid zone (EZ)-line width. PATIENTS AND METHODS: Fundus autofluorescence (FAF) and spectral-domain optical coherence tomography (SD-OCT) images were obtained from seven patients with...

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Identifiers

PMID: 30153077
DOI: 10.1080/13816810.2018.1509354

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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