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Article

Correlation of clinical and genetic findings in Hungarian patients with Stargardt disease.

Investigative ophthalmology & visual science - 1 Dec 2005

Hargitai Janos, Zernant Jana, Somfai Gabor M, Vamos Rita, Farkas Agnes, Salacz Gyorgy, Allikmets Rando

Abstract excerpt

PURPOSE: Autosomal recessive Stargardt disease (arSTGD) presents with substantial clinical and genetic heterogeneity. This study was conducted to correlate foveolar thickness (FT) and total macular volume (TMV), measured by optical coherence tomography (OCT), with other clinical characteristics and with specific genetic variation in Hungarian patients with arSTGD. METHODS: After a standard ophthalmic workup, both...

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Source

Identifiers

PMID: 16303926
DOI: 10.1167/iovs.05-0504

Genes

ABCA4

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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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