Literature DB >> 1449769

Leber hereditary optic neuropathy in Australia.

D A Mackey1, R G Buttery.   

Abstract

Leber hereditary optic neuropathy (LHON) presents with sudden onset of visual loss mainly in young adult males. LHON is not uncommon in Australia, accounting for 2% of invalid blind pensions. We have identified 20 unrelated families carrying mitochondrial DNA mutations associated with LHON and 135 of 291 individuals with documented LHON are currently alive in Australia. The mean age of onset of visual loss for males was 26 years and for females 27 years, with a range from six to 65 years. The mean risk of visual loss was 20% for males and 4% for females. There are over 1750 male and female carriers living in Australia who have not yet lost vision; 600 carriers are under 24 years of age. The expected number of new cases of blindness from LHON is three to four per year.

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Year:  1992        PMID: 1449769     DOI: 10.1111/j.1442-9071.1992.tb00937.x

Source DB:  PubMed          Journal:  Aust N Z J Ophthalmol        ISSN: 0814-9763


  21 in total

1.  The pedigree rate of sequence divergence in the human mitochondrial genome: there is a difference between phylogenetic and pedigree rates.

Authors:  Neil Howell; Christy Bogolin Smejkal; D A Mackey; P F Chinnery; D M Turnbull; Corinna Herrnstadt
Journal:  Am J Hum Genet       Date:  2003-02-04       Impact factor: 11.025

2.  The epidemiology of Leber hereditary optic neuropathy in the North East of England.

Authors:  P Yu-Wai-Man; P G Griffiths; D T Brown; N Howell; D M Turnbull; P F Chinnery
Journal:  Am J Hum Genet       Date:  2002-01-07       Impact factor: 11.025

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.  How rapidly does the human mitochondrial genome evolve?

Authors:  N Howell; I Kubacka; D A Mackey
Journal:  Am J Hum Genet       Date:  1996-09       Impact factor: 11.025

5.  Clustering of Caucasian Leber hereditary optic neuropathy patients containing the 11778 or 14484 mutations on an mtDNA lineage.

Authors:  M D Brown; F Sun; D C Wallace
Journal:  Am J Hum Genet       Date:  1997-02       Impact factor: 11.025

6.  The role of the Met98Lys optineurin variant in inherited optic nerve diseases.

Authors:  J E Craig; A W Hewitt; D P Dimasi; N Howell; C Toomes; A C Cohn; D A Mackey
Journal:  Br J Ophthalmol       Date:  2006-08-02       Impact factor: 4.638

7.  When does bilateral optic atrophy become Leber hereditary optic neuropathy?

Authors:  N Howell; S Halvorson; J Burns; D A McCullough; J Paulton
Journal:  Am J Hum Genet       Date:  1993-10       Impact factor: 11.025

8.  Longitudinal study of a heteroplasmic 3460 Leber hereditary optic neuropathy family by multiplexed primer-extension analysis and nucleotide sequencing.

Authors:  S S Ghosh; E Fahy; I Bodis-Wollner; J Sherman; N Howell
Journal:  Am J Hum Genet       Date:  1996-02       Impact factor: 11.025

9.  Finger prick blood testing in Leber hereditary optic neuropathy.

Authors:  D Mackey; S Nasioulas; S Forrest
Journal:  Br J Ophthalmol       Date:  1993-05       Impact factor: 4.638

10.  Identification of novel mitochondrial mutations in Leber's hereditary optic neuropathy.

Authors:  Manoj Kumar; Mukesh Tanwar; Rohit Saxena; Pradeep Sharma; Rima Dada
Journal:  Mol Vis       Date:  2010-04-30       Impact factor: 2.367

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