Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Recurrent granular dystrophy of the cornea: an unusual case.

Cornea - 1 Jun 2006

Frising Martine, Wildhardt Gabriele, Frisch Lars, Pitz Susanne

Abstract excerpt

PURPOSE: To describe a case of severe corneal granular dystrophy with clinicopathologic and molecular genetic findings. METHODS: The DNAs of a 53-year-old male patient suffering from corneal granular dystrophy and nonaffected family members were analyzed by molecular genetic methods. Clinical features, and histopathologic and immunohistochemical findings from the penetrating keratoplasty specimen, are described....

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Exons
Share to Corneal Dystrophies, Hereditary
Share to DNA Mutational Analysis

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Extracellular Matrix Proteins

Share to Molecular Biology

Share to Polymerase Chain Reaction

Share to Recurrence

Share to Transforming Growth Factor beta

Source

Identifiers

PMID: 16783153
DOI: 10.1097/01.ico.0000214202.84081.a5

Provenance

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.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Recurrent granular dystrophy of the cornea: an unusual case.PMID 16783153Read ↗

Unusual early recurrence of granular dystrophy after deep anterior lamellar keratoplasty: case report.Semantic proximity Read ↗

Granular corneal dystrophy: an enigma resolved.Semantic proximity Read ↗

Granular corneal dystrophy with homozygous mutations in the kerato-epithelin gene.Semantic proximity Read ↗

Genotype-phenotype correlation in 2 Indian families with severe granular corneal dystrophy.Semantic proximity Read ↗

Bilateral Atypical Granular Corneal Dystrophy Associated with Unilateral Keratoconus in a Male Child.Semantic proximity Read ↗

An autosomal dominant granular corneal dystrophy family associated with R555W mutation in the BIGH3 gene.Semantic proximity Read ↗

The phenotype of arg555trp mutation in a large Turkish family with corneal granular dystrophy.Semantic proximity Read ↗

A new corneal disease with recurrent erosive episodes and autosomal-dominant inheritance.Semantic proximity Read ↗

Corneal decompensation in recessive cornea plana.Semantic proximity Read ↗

[Early recurrence of Groenouw type I corneal dystrophy after phototherapeutic keratectomy. Molecular biology study suggests epithelial genesis].Semantic proximity Read ↗

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

A case of concomitant keratoconus and granular corneal dystrophy type II.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.