Literature DB >> 16083845

Hereditary optic neuropathies: from the mitochondria to the optic nerve.

Nancy J Newman1.   

Abstract

PURPOSE: To review our current knowledge of inherited optic neuropathies.
DESIGN: Perspective.
METHODS: Literature review.
RESULTS: The hereditary optic neuropathies consist of a group of disorders in which optic nerve dysfunction figures solely or prominently and direct inheritance is clinically or genetically proven. The most common of these disorders are autosomal dominant optic atrophy (Kjers' disease) and maternally-inherited Leber's hereditary optic neuropathy. Other inherited neurologic and systemic syndromic diseases will frequently manifest optic neuropathy. A selective vulnerability of the optic nerve to perturbations in mitochondrial function may underlie a final common pathway among these disorders.
CONCLUSIONS: The ophthalmologist should be familiar with the clinical characteristics and diagnosis of the hereditary optic neuropathies. Recent advances in our understanding of the underlying pathophysiology of the inherited optic neuropathies may provide insight into their treatment and the treatment of acquired optic nerve disorders.

Entities:  

Mesh:

Year:  2005        PMID: 16083845     DOI: 10.1016/j.ajo.2005.03.017

Source DB:  PubMed          Journal:  Am J Ophthalmol        ISSN: 0002-9394            Impact factor:   5.258


  51 in total

1.  Leber's hereditary optic neuropathy associated with cocaine, ecstasy and telithromycin consumption.

Authors:  Elena Cardaioli; Paola Da Pozzo; Gian Nicola Gallus; Rossella Franceschini; Alessandra Rufa; Maria Teresa Dotti; Aldo Caporossi; Antonio Federico
Journal:  J Neurol       Date:  2007-03-02       Impact factor: 4.849

2.  Increased relative mitochondrial DNA content in leucocytes of patients with NAION.

Authors:  K K Abu-Amero; T M Bosley
Journal:  Br J Ophthalmol       Date:  2006-03-15       Impact factor: 4.638

Review 3.  The neuro-ophthalmology of mitochondrial disease.

Authors:  J Alexander Fraser; Valérie Biousse; Nancy J Newman
Journal:  Surv Ophthalmol       Date:  2010-05-14       Impact factor: 6.048

4.  Leber's hereditary optic neuropathy (LHON) in an Apulian cohort of subjects.

Authors:  Angelica Bianco; Luigi Bisceglia; Paolo Trerotoli; Luciana Russo; Leonardo D'Agruma; Silvana Guerriero; Vittoria Petruzzella
Journal:  Acta Myol       Date:  2017-09-01

5.  Weighing in on Leber hereditary optic neuropathy: effects of mitochondrial mass.

Authors:  Michio Hirano
Journal:  Brain       Date:  2014-02       Impact factor: 13.501

6.  Altered axonal mitochondrial transport in the pathogenesis of Charcot-Marie-Tooth disease from mitofusin 2 mutations.

Authors:  Robert H Baloh; Robert E Schmidt; Alan Pestronk; Jeffrey Milbrandt
Journal:  J Neurosci       Date:  2007-01-10       Impact factor: 6.167

7.  Clinical approach to optic neuropathies.

Authors:  Raed Behbehani
Journal:  Clin Ophthalmol       Date:  2007-09

8.  Bilateral vision loss due to Leber's hereditary optic neuropathy after long-term alcohol, nicotine and drug abuse.

Authors:  Johanna Maass; Egbert Matthé
Journal:  Doc Ophthalmol       Date:  2018-01-25       Impact factor: 2.379

9.  Inhibition of TFG function causes hereditary axon degeneration by impairing endoplasmic reticulum structure.

Authors:  Christian Beetz; Adam Johnson; Amber L Schuh; Seema Thakur; Rita-Eva Varga; Thomas Fothergill; Nicole Hertel; Ewa Bomba-Warczak; Holger Thiele; Gudrun Nürnberg; Janine Altmüller; Renu Saxena; Edwin R Chapman; Erik W Dent; Peter Nürnberg; Anjon Audhya
Journal:  Proc Natl Acad Sci U S A       Date:  2013-03-11       Impact factor: 11.205

10.  Autosomal dominant optic neuropathy and sensorineual hearing loss associated with a novel mutation of WFS1.

Authors:  Barend F T Hogewind; Ronald J E Pennings; Frans A Hol; Henricus P M Kunst; Elisabeth H Hoefsloot; Johannes R M Cruysberg; Cor W R J Cremers
Journal:  Mol Vis       Date:  2010-01-12       Impact factor: 2.367

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