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

Classic lattice corneal dystrophy associated with monoclonal gammopathy after exclusion of a TGFBI mutation.

Cornea - 1 Jan 2009

Kamal Khairidzan M, Rayner Sylvia A, Chen Michael C, Aldave Anthony J

Abstract excerpt

PURPOSE: The purpose of this study was to report the association of phenotypic features characteristic of lattice corneal dystrophy (LCD) with a monoclonal gammopathy of undetermined significance (MGUS) after exclusion of a coding region mutation in transforming growth factor beta-induced (TGFBI) gene. DESIGN: Case report. METHODS: Slit-lamp examination and collection of DNA for TGFBI screening were performed. A...

Read the complete abstract on PubMed

Topics

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

Share to Blood Proteins
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 Electrophoresis

Share to Extracellular Matrix Proteins

Share to Paraproteinemias

Share to Transforming Growth Factor beta

Source

Open in PubMed Open full text

Identifiers

PMID: 19092416
DOI: 10.1097/ICO.0b013e31818200f4
PMCID: PMC2784604

Genes

TGFBI

Variants

rs1442
rs1054124
rs1133170

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

Classic lattice corneal dystrophy associated with monoclonal gammopathy after exclusion of a TGFBI mutation.PMID 19092416Read ↗

Variant lattice corneal dystrophy associated with compound heterozygous mutations in the TGFBI gene.Semantic proximity Read ↗

Late-Onset Lattice Corneal Dystrophy Without Typical Lattice Lines Caused by a Novel Mutation in the TGFBI GeneSemantic proximity Read ↗

Heavy-chain amyloidosis in TGFBI-negative and gelsolin-negative atypical lattice corneal dystrophy.Semantic proximity Read ↗

A novel variant of combined granular-lattice corneal dystrophy associated with the Met619Lys mutation in the TGFBI gene.Semantic proximity Read ↗

Two mutations in the TGFBI (BIGH3) gene associated with lattice corneal dystrophy in an extensively studied family.Semantic proximity Read ↗

Lattice corneal dystrophy type IIIA with hyaline component from a novel A620P mutation and distinct surgical treatments.Semantic proximity Read ↗

The TGFBI A546D mutation causes an atypical type of lattice corneal dystrophy.Semantic proximity Read ↗

A novel missense TGFBI variant p.(Ser591Phe) in a Finnish family with variant lattice corneal dystrophy.Semantic proximity Read ↗

A novel TGFBI phenotype with amyloid deposits and Arg124Leu mutation.Semantic proximity Read ↗

Genotype-Phenotype Correlation for TGFBI Corneal Dystrophies Identifies p.(G623D) as a Novel Cause of Epithelial Basement Membrane Dystrophy.Semantic proximity Read ↗

Late-onset Form of Lattice Corneal Dystrophy Caused by Leu527Arg Mutation of the TGFBI GeneSemantic proximity Read ↗

Clinical and genetic features of TGFBI-linked corneal dystrophies in Mexican population: description of novel mutations and novel genotype-phenotype correlations.Semantic proximity Read ↗

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