A Typical Case Presentation with Spontaneous Visual Recovery in Patient Diagnosed with Leber Hereditary Optic Neuropathy due to Rare Point Mutation in <i>MT-ND4</i> Gene (<i>m.11253T>C</i>) and Literature Review

A Typical Case Presentation with Spontaneous Visual Recovery in Patient Diagnosed with Leber Hereditary Optic Neuropathy due to Rare Point Mutation in <i>MT-ND4</i> Gene (<i>m.11253T>C</i>) and Literature Review

Leber hereditary optic neuropathy (LHON) is one of the most common inherited mitochondrial optic neuropathies, caused by mitochondrial DNA (mtDNA) mutations. Three most common mutations, namely <i>m.11778G>A</i>, <i>m.14484T>G</i> and <i>m.3460G>A</i>, ac...

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Bibliographic Details
Main Authors: Rasa Liutkeviciene, Agne Sidaraite, Lina Kuliaviene, Brigita Glebauskiene, Neringa Jurkute, Lina Aluzaite-Baranauskiene, Arvydas Gelzinis, Reda Zemaitiene
Format: Article
Language:English
Published: MDPI AG 2021-02-01
Series:Medicina
Subjects:
Leber hereditary optic neuropathy
LHON
aetiology
diagnosis
treatment
Online Access:https://www.mdpi.com/1010-660X/57/3/202

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