Journal of Neuro-Ophthalmology · 2016 · 19 citations · 13 references
MedicineNeurologyOphthalmologyHuman GeneticsMitochondrial GeneticsNeurogeneticsGenetic DisordersHereditary NeuropathiesMitochondrial DiseaseMitochondrial DisordersMitochondrial Ocular DisordersOptic NeuropathiesHereditary Eye DiseaseHereditary Ocular DiseaseInherited Ocular DiseaseInherited Ocular DisordersInherited Optic NeuropathiesLeber Hereditary Optic NeuropathyPediatric Optic Neuropathies
A 5-year-old boy developed profound loss of vision in his right eye and was found to have a 11778 mitochondrial point mutation consistent with Leber hereditary optic neuropathy (LHON). He maintained 20/20 vision in the left eye for 18 years until age 23, when he experienced loss of vision in that eye. This 18 year interval between eye involvement in LHON is the longest reported to date and reinforces the variability in presentation and progression seen in this disease.
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Gene–environment interactions in Leber hereditary optic neuropathy
Matthew A. Kirkman, Patrick Yu‐Wai‐Man, Alex Korsten et al. · Brain · 2009 · 355 citations · Full text
Carla Giordano, Luisa Iommarini, Luca Giordano et al. · Brain · 2013 · 285 citations · Full text
Life Sciences, Biology, Genetics +16
Leber’s Hereditary Optic Neuropathy with Childhood Onset
Piero Barboni, Giacomo Savini, Maria Lucia Valentino et al. · Investigative Ophthalmology & Visual Science · 2006 · 147 citations
Medicine, Neurology, Ophthalmology +17