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

Posterior amorphous corneal dystrophy. A new pedigree with phenotypic variation.

Ophthalmology - 1 Mar 1996

Moshegov C N, Hoe W K, Wiffen S J, Daya S M

Abstract excerpt

BACKGROUND: Posterior amorphous corneal dystrophy is a rare condition characterized by bilateral sheet-like opacification of the posterior stroma in association with corneal flattening and thinning. It has been reported in only four families, all from the United States. The authors report on a fifth family, the first from Britain, with nine affected individuals. METHODS: Slit-lamp photography, refraction,...

Read the complete abstract on PubMed

Topics

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

Share to Adolescent
Share to Aged
Share to Child

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Cornea

Share to Genetic Variation

Share to Image Processing, Computer-Assisted

Share to Pedigree

Share to Phenotype

Source

Identifiers

PMID: 8600425
DOI: 10.1016/s0161-6420(96)30669-6

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Posterior amorphous corneal dystrophy. A new pedigree with phenotypic variation.PMID 8600425Read ↗

Corneal ectasia associated with posterior lamellar opacification.Semantic proximity Read ↗

Linkage of posterior amorphous corneal dystrophy to chromosome 12q21.33 and exclusion of coding region mutations in KERA, LUM, DCN, and EPYC.Semantic proximity Read ↗

Posterior Amorphous Corneal Dystrophy Is Associated with a Deletion of Small Leucine-rich Proteoglycans on Chromosome 12Semantic proximity Read ↗

Confirmation and refinement of the heterozygous deletion of the small leucine-rich proteoglycans associated with posterior amorphous corneal dystrophy.Semantic proximity Read ↗

Novel corneal phenotype in a patient with alport syndrome.Semantic proximity Read ↗

Clinical and molecular analysis of children with central pulverulent cataract from the Arabian Peninsula.Semantic proximity Read ↗

Clinical phenotype of posterior polymorphous corneal dystrophy in a family with a novel ZEB1 mutation.Semantic proximity Read ↗

Familial peripheral keratopathy without PAX6 mutation.Semantic proximity Read ↗

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

Individual phenotypic variances in a family with Thiel-Behnke corneal dystrophy.Semantic proximity Read ↗

Posterior Polymorphous Corneal Dystrophy in a Patient with a Novel ZEB1 Gene Mutation.Semantic proximity Read ↗

Variable Phenotype of Congenital Corneal Opacities in Biallelic CYP1B1 Pathogenic Variants.Semantic proximity Read ↗

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