| Leber's hereditary optic neuropathy |
Leber’s hereditary optic neuropathy (LHON) or Leber optic atrophy (LOA) is a maternally inherited form of acute or subacute loss of central vision that may lead to degeneration of retinal ganglion cells (RGCs) and their axons; this affects predominantly young adult males. However, LHON is only transmitted through the mother as it is primarily due to mutations in the mitochondrial (not nuclear) genome and only the egg contributes mitochondria to the embryo. ...
출처: en.wikipedia.org/wiki/Leber's_hereditary_optic...
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| Leber's disease |
a rare form of inherited juvenile macular degeneration characterized by optic atrophy in both eyes (bilateral) and leading to reduction of vision. For more information, see "Eye Diseases" on the MD Support web site.
출처: www.mdsupport.org/glossary.html
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| Leber's congenital a. |
a. congenita.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| Leber's congenital amaurosis, etc. |
see amaurosis congenita, under amaurosis, Hassall's corpuscles, under corpuscle, and Hovius' plexus, under plexus; and see under neuropathy.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| Leber's d. |
1. Leber's hereditary optic neuropathy. 2. Leber's congenital amaurosis.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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