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Article

[Autosomal dominant granular corneal dystrophy caused by a TGFBI gene mutation in a Mexican family].

Archivos de la Sociedad Espanola de Oftalmologia - 1 Jul 2006

Zenteno J C, Santacruz-Valdés C, Ramírez-Miranda A

Abstract excerpt

OBJECTIVE: To describe the clinical data and the results of molecular analyses of the TGFBI gene in a patient with classic granular stromal corneal dystrophy (type I). METHODS: A female patient aged 60-years complaining of a long-standing decrease of visual acuity bilaterally associated with phot...

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Share to Corneal Dystrophies, Hereditary
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 16888689
DOI: 10.4321/s0365-66912006000700004

Genes

TGFBI

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-16888689-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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[Autosomal dominant granular corneal dystrophy caused by a TGFBI gene mutation in a Mexican family].PMID 16888689Read ↗

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