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

Dystrophia Helsinglandica: a new type of hereditary corneal recurrent erosions with late subepithelial fibrosis.

Acta ophthalmologica - 1 Sept 2009

Hammar Björn, Björck Erik, Lind Helena, Lagerstedt Kristina, Dellby Anette, Fagerholm Per

Abstract excerpt

PURPOSE: To describe the phenotype of an autosomal-dominant corneal dystrophy with an early onset of recurrent corneal erosions and development of subepithelial fibrosis in the cornea, and also to exclude genetic linkage to known corneal dystrophies with autosomal-dominant inheritance and clinica...

Read the complete abstract on PubMed

Topics

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

Share to Cornea
Share to Corneal Dystrophies, Hereditary
Share to Epithelium, Corneal

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Fibrosis

Share to Medical Records

Share to Molecular Biology

Share to Recurrence

Share to Visual Acuity

Source

Identifiers

PMID: 18700883
DOI: 10.1111/j.1755-3768.2008.01308.x

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-18700883-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Dystrophia Helsinglandica: a new type of hereditary corneal recurrent erosions with late subepithelial fibrosis.PMID 18700883Read ↗

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

[Masquerade keratitis due to hereditary corneal disorders].Semantic proximity Read ↗

A COL17A1 Splice-Altering Mutation Is Prevalent in Inherited Recurrent Corneal Erosions.Semantic proximity Read ↗

Phenotypic variability in Meesmann's dystrophy: clinical review of the literature and presentation of a family genetically identical to the original family.Semantic proximity Read ↗

Mutations in collagen, type XVII, alpha 1 (COL17A1) cause epithelial recurrent erosion dystrophy (ERED).Semantic proximity Read ↗

Matrix Metalloproteinases and the Pathogenesis of Recurrent Corneal Erosions and Epithelial Basement Membrane DystrophySemantic proximity Read ↗

Early and late clinical landmarks of corneal dystrophies.Semantic proximity Read ↗

Genetics of Anterior and Stromal Corneal DystrophiesSemantic proximity Read ↗

Recurrent granular dystrophy of the cornea: an unusual case.Semantic proximity Read ↗

Phenotypic variation in combined granular-lattice (Avellino) corneal dystrophy.Semantic proximity Read ↗

Stepwise treatment stratagem of young patient with Reis–Bücklers corneal dystrophy: A case reportSemantic proximity Read ↗

Peripheral hypertrophic subepithelial corneal degeneration: nomenclature, phenotypes, and long-term outcomes.Semantic proximity Read ↗

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