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

The epidemiology and mutation types of Leber's hereditary optic neuropathy in Thailand.

Annals of medicine - 1 Dec 2022

Sathianvichitr Kanchalika, Sigkaman Benjaporn, Chirapapaisan Niphon, Laowanapiban Poramaet, Padungkiatsagul Tanyatuth, Apinyawasisuk Supanut, Witthayaweerasak Juthamat, Chuenkongkaew Wanicha

Abstract excerpt

PURPOSE: Leber's hereditary optic neuropathy (LHON), the most common mitochondrial optic neuropathy, causes visual loss, especially in young adults. Due to the absence of epidemiological data in Southeast Asia, we aimed to determine Thai LHON patients' characteristics (demographic data, mutation types, and prognoses) as the first study in this region. METHODS: This retrospective chart review enrolled all Thai...

Read the complete abstract on PubMed

Topics

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

Share to DNA, Mitochondrial
Share to Mutation

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Optic Atrophy, Hereditary, Leber

Share to Pedigree

Share to Thailand

Share to Young Adult

Source

Open in PubMed Open full text

Identifiers

PMID: 35723074
DOI: 10.1080/07853890.2022.2082517
PMCID: PMC9191831

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

The epidemiology and mutation types of Leber's hereditary optic neuropathy in Thailand.PMID 35723074Read ↗

The unique characteristics of Thai Leber hereditary optic neuropathy: analysis of 30 G11778A pedigrees.Semantic proximity Read ↗

Leber's Hereditary Optic Neuropathy with Mitochondrial DNA Mutation G11778A: A Systematic Literature Review and Meta-Analysis.Semantic proximity Read ↗

Variant and clinical landscape of Leber hereditary optic neuropathy based on 1516 families with mtDNA variants in a tertiary centre.Semantic proximity Read ↗

Meta-analysis of the prevalence of Leber hereditary optic neuropathy mtDNA mutations in Europe.Semantic proximity Read ↗

Leber's hereditary optic neuropathy in Thailand.Semantic proximity Read ↗

Nationwide epidemiological survey of Leber hereditary optic neuropathy in Japan.Semantic proximity Read ↗

Clinical features of Leber's hereditary optic neuropathy with the 11778 mitochondrial DNA mutation in Taiwanese patients.Semantic proximity Read ↗

Genotypic and phenotypic characteristics of Korean children with childhood-onset Leber's hereditary optic neuropathy.Semantic proximity Read ↗

A hospital-based five-year prospective study on the prevalence of Leber's hereditary optic neuropathy with genetic confirmation.Semantic proximity Read ↗

[Clinical practice guidelines for Leber's hereditary optic neuropathy].Semantic proximity Read ↗

Pathogenic mitochondrial DNA mutations and associated clinical features in Korean patients with Leber's hereditary optic neuropathy.Semantic proximity Read ↗

Analysis of secondary mtDNA mutations in families with Leber's hereditary optic neuropathy: Four novel variants and their association with clinical presentation.Semantic proximity Read ↗

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