Leberhereditaryopticneuropathyomim

由PYu-Wai-Man著作·2021·被引用135次—Leberhereditaryopticneuropathy(LHON)typicallypresentsinyoungadultsasbilateral,painless,subacutevisualfailure.ThepeakageofonsetinLHON ...,AutosomalrecessiveLeberhereditaryopticneuropathy-1(LHONAR1)ischaracterizedbybilateralsynchronousorasynchronousvisionlosswithvariable ...,Leberopticatrophy,alsoknownasLeberhereditaryopticatrophy(LHON;535000),ischaracterizedby...

參考資訊如下
Leber Hereditary Optic Neuropathy

由 P Yu-Wai-Man 著作 · 2021 · 被引用 135 次 — Leber hereditary optic neuropathy (LHON) typically presents in young adults as bilateral, painless, subacute visual failure. The peak age of onset in LHON ...

619382

Autosomal recessive Leber hereditary optic neuropathy-1 (LHONAR1) is characterized by bilateral synchronous or asynchronous vision loss with variable ...

LEBER HEREDITARY OPTIC NEUROPATHY, MODIFIER ...

Leber optic atrophy, also known as Leber hereditary optic atrophy (LHON; 535000), is characterized by bilateral, painless, subacute central vision loss in young ...

Entry - #535000

LHON presents in midlife as acute or subacute central vision loss leading to central scotoma and blindness. The disease has been associated with many ...

Entry - #619382 - LEBER

Autosomal recessive Leber-like hereditary optic neuropathy-1 (LHONAR1) is characterized by bilateral synchronous or asynchronous vision loss with variable ...

Entry - #500001

NOTE: OMIM is intended for use primarily by physicians and other professionals concerned with genetic disorders, by genetics researchers, and by advanced ...