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

Corneal ectasia associated with posterior lamellar opacification.

Ophthalmic genetics - 1 Aug 2021

Yung Madeline, Chen Angela C, Chung Doug D, Barrington Alice, Zhang Junwei, Frausto Ricardo F, Magalhaes Otavio A, Aldave Anthony J

Abstract excerpt

BACKGROUND: Concomitant corneal ectasia and posterior lamellar corneal opacification is rare, and the genetic relationship between these two conditions is unclear. We report the genetic and clinical characterization of this phenotype in three unrelated individuals. MATERIALS AND METHODS: One previously reported affected individual and two unreported, unrelated, affected individuals were recruited for the study....

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

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Corneal Opacity

Share to Corneal Stroma

Share to Dilatation, Pathologic

Share to Joint Instability

Share to Keratoconus

Share to Skin Abnormalities

Source

Identifiers

PMID: 34003075
DOI: 10.1080/13816810.2021.1923034

Provenance

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.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Corneal ectasia associated with posterior lamellar opacification.PMID 34003075Read ↗

Posterior amorphous corneal dystrophy. A new pedigree with phenotypic variation.Semantic proximity Read ↗

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

Posterior Amorphous Corneal Dystrophy Is Associated with a Deletion of Small Leucine-rich Proteoglycans on Chromosome 12Semantic 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 polymorphous corneal dystrophy 3 is associated with agenesis and hypoplasia of the corpus callosum.Semantic proximity Read ↗

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

Chromosome abnormalities and the genetics of congenital corneal opacification.Semantic proximity Read ↗

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

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

Clinical and molecular characterization of a family with autosomal recessive cornea plana.Semantic proximity Read ↗

Phenotypic characterisation and ZEB1 mutational analysis in posterior polymorphous corneal dystrophy in a New Zealand population.Semantic proximity Read ↗

Ocular Phenotype of Peters-Plus Syndrome.Semantic proximity Read ↗

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