Literature DB >> 15534600

Hereditary optic neuropathies.

N J Newman1, V Biousse.   

Abstract

AIMS: To provide a clinical update on the hereditary optic neuropathies.
METHODS: Review of the literature.
RESULTS: The hereditary optic neuropathies comprise a group of disorders in which the cause of optic nerve dysfunction appears to be hereditable, based on familial expression or genetic analysis. In some hereditary optic neuropathies, optic nerve dysfunction is typically the only manifestation of the disease. In others, various neurologic and systemic abnormalities are regularly observed.
CONCLUSION: The most common hereditary optic neuropathies are autosomal dominant optic atrophy (Kjer's disease) and maternally inherited Leber's hereditary optic neuropathy. We review the clinical phenotypes of these and other inherited disorders with optic nerve involvement.

Entities:  

Mesh:

Year:  2004        PMID: 15534600     DOI: 10.1038/sj.eye.6701591

Source DB:  PubMed          Journal:  Eye (Lond)        ISSN: 0950-222X            Impact factor:   3.775


  44 in total

Review 1.  A hypothesis to suggest that light is a risk factor in glaucoma and the mitochondrial optic neuropathies.

Authors:  N N Osborne; G Lascaratos; A J Bron; G Chidlow; J P M Wood
Journal:  Br J Ophthalmol       Date:  2006-02       Impact factor: 4.638

2.  [Hereditary optic atrophies].

Authors:  C M Poloschek; W A Lagrèze
Journal:  Ophthalmologe       Date:  2009-09       Impact factor: 1.059

3.  Clinical neuro-ophthalmic findings in familial dysautonomia.

Authors:  Carlos E Mendoza-Santiesteban; Thomas R Hedges; Lucy Norcliffe-Kaufmann; Floyd Warren; Shantan Reddy; Felicia B Axelrod; Horacio Kaufmann
Journal:  J Neuroophthalmol       Date:  2012-03       Impact factor: 3.042

4.  Late-onset Leber's hereditary optic neuropathy: the role of environmental factors in hereditary diseases.

Authors:  Nuno Moura-Coelho; Rita Pinto Proença; Joana Tavares Ferreira; João Paulo Cunha
Journal:  BMJ Case Rep       Date:  2019-03-20

5.  Atypical Leber's hereditary optic neuropathy in a 10-year-old male: a case report.

Authors:  Yung Ju Yoo; Hee Kyung Yang; Jeong-Min Hwang
Journal:  Neurol Sci       Date:  2017-07-29       Impact factor: 3.307

6.  Heterozygous deletion of the OPA1 gene in patients with dominant optic atrophy.

Authors:  Takaaki Hayashi; Hiroyuki Sasano; Satoshi Katagiri; Kazushige Tsunoda; Shuhei Kameya; Mitsuru Nakazawa; Takeshi Iwata; Hiroshi Tsuneoka
Journal:  Jpn J Ophthalmol       Date:  2017-07-01       Impact factor: 2.447

7.  [Differential diagnosis of juvenile normal pressure glaucoma].

Authors:  K Geidel; P Wiedemann; J D Unterlauft
Journal:  Ophthalmologe       Date:  2017-09       Impact factor: 1.059

8.  Multi-system neurological disease is common in patients with OPA1 mutations.

Authors:  P Yu-Wai-Man; P G Griffiths; G S Gorman; C M Lourenco; A F Wright; M Auer-Grumbach; A Toscano; O Musumeci; M L Valentino; L Caporali; C Lamperti; C M Tallaksen; P Duffey; J Miller; R G Whittaker; M R Baker; M J Jackson; M P Clarke; B Dhillon; B Czermin; J D Stewart; G Hudson; P Reynier; D Bonneau; W Marques; G Lenaers; R McFarland; R W Taylor; D M Turnbull; M Votruba; M Zeviani; V Carelli; L A Bindoff; R Horvath; P Amati-Bonneau; P F Chinnery
Journal:  Brain       Date:  2010-02-15       Impact factor: 13.501

9.  OPA1 mutations cause cytochrome c oxidase deficiency due to loss of wild-type mtDNA molecules.

Authors:  Patrick Yu-Wai-Man; Kamil S Sitarz; David C Samuels; Philip G Griffiths; Amy K Reeve; Laurence A Bindoff; Rita Horvath; Patrick F Chinnery
Journal:  Hum Mol Genet       Date:  2010-05-18       Impact factor: 6.150

10.  Gene-environment interactions in Leber hereditary optic neuropathy.

Authors:  Matthew Anthony Kirkman; Patrick Yu-Wai-Man; Alex Korsten; Miriam Leonhardt; Konstantin Dimitriadis; Ireneaus F De Coo; Thomas Klopstock; Patrick Francis Chinnery
Journal:  Brain       Date:  2009-06-12       Impact factor: 13.501

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