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

Long-Term Outcome After Penetrating Keratoplasty in a Pedigree With the G177E Mutation in the UBIAD1 Gene for Schnyder Corneal Dystrophy.

Cornea - 1 May 2018

Kitazawa Koji, Wakimasu Koichi, Kayukawa Kanae, Sugimoto Manabu, Nakai Junko, Weiss Jayne S, Ueno Morio, Sotozono Chie, Kinoshita Shigeru

Abstract excerpt

PURPOSE: To investigate the long-term surgical outcome after penetrating keratoplasty in 5 patients from 1 pedigree with Schnyder corneal dystrophy (SCD), resulting from the same UbiA prenyltransferase domain containing 1 (UBIAD1) mutation. METHODS: This retrospective study involved 6 eyes of 5 patients who underwent penetrating keratoplasty for treatment of SCD. Postoperative surgical outcome measures included...

Read the complete abstract on PubMed

Topics

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

Share to Aged
Share to Corneal Dystrophies, Hereditary

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to DNA Mutational Analysis

Share to SCD gene

Share to Graft Rejection

Share to Mutation

Share to Pedigree

Share to Recurrence

Source

Identifiers

PMID: 29319599
DOI: 10.1097/ICO.0000000000001511

Genes

UBIAD1
SCD

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Long-Term Outcome After Penetrating Keratoplasty in a Pedigree With the G177E Mutation in the UBIAD1 Gene for Schnyder Corneal Dystrophy.PMID 29319599Read ↗

UbiA prenyltransferase domain-containing protein 1 (UBIAD1) variant c.695 A > G identified in a multigenerational Japanese family with Schnyder corneal dystrophy.Semantic proximity Read ↗

Surgical management and genetic analysis of a Chinese family with the S171P mutation in the UBIAD1 gene, the gene for Schnyder corneal dystrophy.Semantic proximity Read ↗

A mutation in the UBIAD1 gene in a Han Chinese family with Schnyder corneal dystrophy.Semantic proximity Read ↗

Clinical diversity in patients with Schnyder corneal dystrophy-a novel and known UBIAD1 pathogenic variants.Semantic proximity Read ↗

Mutational spectrum of Korean patients with corneal dystrophy.Semantic proximity Read ↗

UBIAD1 mutation alters a mitochondrial prenyltransferase to cause Schnyder corneal dystrophy.Semantic proximity Read ↗

Mutations in the UBIAD1 gene on chromosome short arm 1, region 36, cause Schnyder crystalline corneal dystrophy.Semantic proximity Read ↗

Fuchs endothelial corneal dystrophy: current perspectivesSemantic proximity Read ↗

CHST6-related macular corneal dystrophy: a matter of endotheliumSemantic proximity Read ↗

In vivo laser confocal microscopy findings and mutational analysis for Schnyder's crystalline corneal dystrophy.Semantic proximity Read ↗

A novel UBIAD1 mutation identified in a Chinese family with Schnyder crystalline corneal dystrophy.Semantic proximity Read ↗

Mutations in the UBIAD1 gene, encoding a potential prenyltransferase, are causal for Schnyder crystalline corneal dystrophy.Semantic proximity Read ↗

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