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Leber optic atrophy

LHON
Leber hereditary optic neuropathy
Optic atrophy, Leber type
[Clinical features: central vision loss leading to central scotoma]
[Inheritance: mitochondrial]

19 images
[ from 1 to 15 ]
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Neuropathology of white matter disease in Leber's hereditary optic neuropathy
Neuropathology of white matter disease in Leber's hereditary optic neuropathy
Complex I respiratory defect in LHON plus dystonia with no mitochondrial DNA mutation
Brain
Brain
British Journal of Ophthalmology

Human extraocular muscles in mitochondrial diseases: comparing chronic progressive external ophthalmoplegia with Leber's hereditary optic neuropathy
Human extraocular muscles in mitochondrial diseases: comparing chronic progressive external ophthalmoplegia with Leber's hereditary optic neuropathy
Human extraocular muscles in mitochondrial diseases: comparing chronic progressive external ophthalmoplegia with Leber's hereditary optic neuropathy
British Journal of Ophthalmology
British Journal of Ophthalmology
British Journal of Ophthalmology

Leber's hereditary optic neuropathy
Leber's hereditary optic neuropathy triggered by antiretroviral therapy for human immunodeficiency virus
Leber's hereditary optic neuropathy triggered by antiretroviral therapy for human immunodeficiency virus
Eye
Eye
Eye

Leber's hereditary optic neuropathy masquerading as ethambutol-induced optic neuropathy in a young male
The Novel A4435G Mutation in the Mitochondrial tRNAMet May Modulate the Phenotypic Expression of the LHON-Associated ND4 G11778A Mutation
Inherited mitochondrial optic neuropathies
Indian Journal of Ophthalmology
Investigative Ophthalmology & Visual Science
Journal of Medical Genetics

Leber hereditary optic neuropathy
Leber hereditary optic neuropathy
Ondine's curse in a woman with Leber's hereditary optic neuropathy
Journal of Medical Genetics
Journal of Medical Genetics
Journal of Neurology, Neurosurgery and Psychiatry

19 images
[ from 1 to 15 ]
1 2 next

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Edited by Aldo Campana, April 19, 2014