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Article

Disruption in Bruch membrane in patients with Stargardt disease.

Ophthalmic genetics - 1 Mar 2012

Park Sung Pyo, Chang Stanley, Allikmets Rando, Smith R Theodore, Burke Tomas R, Gregory-Roberts Emily, Tsang Stephen H

Abstract excerpt

PURPOSE: To describe the spectral domain-optical coherence tomography (SD-OCT) findings of two patients with complete defects in the retinal pigment epithelium (RPE) with disruptions in Bruch membrane in Stargardt disease (STGD1). METHODS: Two patients with STGD1 were referred to our clinic for further evaluation. Fundus autofluorescence (FAF), spectral domain optical coherence tomography (SD-OCT),...

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Source

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Identifiers

PMID: 22060670
DOI: 10.3109/13816810.2011.628358
PMCID: PMC4407800

Genes

ABCA4
RPE
ERG

Provenance

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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