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

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

Molecular vision - 1 Jan 2020

Gowri Poigaialwar, Kumar Shanmugam Mahesh, Vanniarajan Ayyasamy, Bharanidharan Devarajan, Sundaresan Periasamy

Abstract excerpt

Purpose: To estimate the prevalence of Leber hereditary optic neuropathy (LHON) along with genetic screening at a tertiary eye care center in southern India. Methods: Patients with LHON were identified at the Neuro-Ophthalmology Clinic, Aravind Eye Hospital (AEH; Madurai, India) from 2015 to 2019. Clinical data were collected along with blood samples. Genetic testing was performed for the confirmation of LHON...

Read the complete abstract on PubMed

Topics

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

Share to Age of Onset
Share to Genome, Mitochondrial

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

Share to Hospitals

Share to Optic Atrophy, Hereditary, Leber

Share to Polymorphism, Restriction Fragment Length

Share to Prevalence

Share to Tomography, Optical Coherence

Source

Open in PubMed Open full text

Identifiers

PMID: 33380779
PMCID: PMC7769124

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

A hospital-based five-year prospective study on the prevalence of Leber's hereditary optic neuropathy with genetic confirmation.PMID 33380779Read ↗

Prevalence of primary mutations in Leber hereditary optic neuropathy: A five-year report from a tertiary eye care center in India.Semantic proximity Read ↗

Clinical and Genetic Profile of Leber's Hereditary Optic Neuropathy in a Cohort of Patients From a Tertiary Eye Care Center.Semantic proximity Read ↗

Leber hereditary optic neuropathySemantic proximity Read ↗

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

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

Identification of novel mitochondrial mutations in Leber's hereditary optic neuropathy.Semantic proximity Read ↗

Prevalence and Genetics of Leber Hereditary Optic Neuropathy in the Danish Population.Semantic proximity Read ↗

Frequency of primary mutations of Leber's hereditary optic neuropathy patients in North Indian population.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 ↗

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

Leber hereditary optic neuropathy.Semantic proximity Read ↗

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

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