Leber hereditary optic neuropathy (LHON) is an inherited form of vision loss.
genetic conditions
References
Mroczek-Tońska K, Kisiel B, Piechota J, Bartnik E. Leber hereditary opticneuropathy--a disease with a known molecular basis but a mysterious mechanism of pathology. J Appl Genet. 2003;44(4):529-38. Review.
Newman NJ. Hereditary optic neuropathies: from the mitochondria to the opticnerve. Am J Ophthalmol. 2005 Sep;140(3):517-23. Review.
Spruijt L, Kolbach DN, de Coo RF, Plomp AS, Bauer NJ, Smeets HJ, deDie-Smulders CE. Influence of mutation type on clinical expression of Leberhereditary optic neuropathy. Am J Ophthalmol. 2006 Apr;141(4):676-82.
Tońska K, Kodroń A, Bartnik E. Genotype-phenotype correlations in Leberhereditary optic neuropathy. Biochim Biophys Acta. 2010Jun-Jul;1797(6-7):1119-23. doi: 10.1016/j.bbabio.2010.02.032.Review.
Yu-Wai-Man P, Chinnery PF. Leber Hereditary Optic Neuropathy. 2000 Oct 26[updated 2016 Jun 23]. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): Universityof Washington, Seattle; 1993-2020. Available fromhttp://www.ncbi.nlm.nih.gov/books/NBK1174/
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