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PERSPECTIVE article

Front. Neurol.
Sec. Neuro-Ophthalmology
Volume 15 - 2024 | doi: 10.3389/fneur.2024.1466275

Recognizing Leber's hereditary optic neuropathy to avoid delayed diagnosis and misdiagnosis

Provisionally accepted
  • 1 UOC Clinica Neurologica, IRCCS Istituto delle Scienze Neurologiche di Bologna, IRCCS Institute of Neurological Sciences of Bologna (ISNB), Bologna, 40139, Italy
  • 2 San Raffaele Hospital (IRCCS), Milan, Lombardy, Italy
  • 3 San Camillo Forlanini Hospital, Rome, Lazio, Italy
  • 4 Azienda Ospedaliera Ospedali Riuniti Villa Sofia Cervello, Palermo, Sicily, Italy
  • 5 Chiesi Farmaceutici (Italy), Parma, Emilia-Romagna, Italy
  • 6 University of Rome Tor Vergata, Roma, Lazio, Italy

The final, formatted version of the article will be published soon.

    Leber's Hereditary Optic Neuropathy (LHON) is a maternally inherited optic nerve disease primarily caused by mutations in mitochondrial DNA (mtDNA). The peak of onset is typically between 15-30 years, but variability exists. Misdiagnosis, often as inflammatory optic neuritis, delays treatment, compounded by challenges in timely genetic diagnosis. Given the availability of a specific treatment for LHON, its early diagnosis is imperative to ensure therapeutic appropriateness. This work gives an updated guidance about LHON differential diagnosis to clinicians dealing also with multiple sclerosis and neuromyelitis optica spectrum disorders. LHON diagnosis relies on clinical signs and paraclinical evaluations. Differential diagnosis in the acute phase primarily involves distinguishing inflammatory optic neuropathies, considering clinical clues such as ocular pain, fundus appearance and visual recovery. Imaging analysis obtained with Optical Coherence Tomography (OCT) assists clinicians in early recognition of LHON and help avoiding misdiagnosis. Genetic testing for the three most common LHON mutations is recommended initially, followed by comprehensive mtDNA sequencing if suspicion persists despite negative results. We present and discuss crucial strategies for accurate diagnosis and management of LHON cases.A combination of clinical signs and paraclinical examinations is necessary to reach a diagnosis of LHON. To establish the severity and the stage of the disease, the following evaluations are recommended: 1) Measurement of best-corrected visual acuity and color vision 2) Assessment of visual fields (VF) with static or kinetic perimetry 3) Measurement of retinal nerve fiber layer (RNFL) and ganglion cell layer (GCL) thickness with Optical Coherence Tomography (OCT) imaging.

    Keywords: Leber hereditary optic neuropathy (LHON), Optic Nerve, Visual Field, optical coherence tomography (OCT), Retinal ganglion cell (RGC)

    Received: 17 Jul 2024; Accepted: 29 Aug 2024.

    Copyright: © 2024 La Morgia, Cascavilla, De Negri, Romano, Canalini, Rossi, Centonze and Filippi. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

    * Correspondence: Chiara La Morgia, UOC Clinica Neurologica, IRCCS Istituto delle Scienze Neurologiche di Bologna, IRCCS Institute of Neurological Sciences of Bologna (ISNB), Bologna, 40139, Italy

    Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.