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Atypical Leber’s Optic Neuropathy

The diagnosis of Leber’s hereditary optic neuropathy (LHON) in 6 female atypical cases seen at Harvard, Emory, and Johns Hopkins Medical Centers required molecular analysis and demonstration of the 11778 mitochondrial DNA mutation for accurate confirmation.

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Autore principale: J Gordon Millichap
Natura: Artigo
Lingua:Inglês
Pubblicazione: Pediatric Neurology Briefs Publishers 1993-05-01
Serie:Pediatric Neurology Briefs
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Accesso online:https://www.pediatricneurologybriefs.com/articles/2979
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