| LCB | Laboratory of Cancer Biology; Leber congenital blindness; left costal border; lymphomatosis cutis be... |
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| LHON | Leber hereditary optic neuropathy |
| LOA | leave of absence; Leber optic atrophy; left occipitoanterior [fetal position] |
| LCA | Leber Congenital Amaurosis |
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| LHON | Leber hereditary optic neuropathy |
| LHON | Leber hereditary optic neuroretinopathy |
| Leber's hereditary optic atrophy | Hereditary degeneration of the optic nerve and papillomacular bundle with resulting rapid loss of central vision, progressive for several weeks, then usually stationary with permanent central scotoma; age of onset is variable, most often in the third decade; more males than females are affected and transmission is cytoplasmic and strictly on the female side. Mutation on the mitochondrial chromosome involved, which presumably interacts with an X-linked mutant. This mechanism may explain the bizarre sex ratio, which differs significantly from one country to another. (05 Mar 2000) |
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| Leber's idiopathic stellate neuroretinitis | A unilateral neuroretinitis with perifoveal exudates in Henle's nerve fibre layer producing a macular star and spontaneous regression in a few months. Synonym: Leber's idiopathic stellate neuroretinitis. (05 Mar 2000) |
| Leber's idiopathic stellate retinopathy | An inflammation affecting the optic nerve head and the posterior pole of the retina, with cells in the nearby vitreous, usually producing a macular star. Synonym: papilloretinitis. (05 Mar 2000) |
| Leber's plexus | A small venous plexus in the eye between the venous sinuses of the sclera (of Schlemm) and the spaces of the iridocorneal angle (of Fontana). (05 Mar 2000) |
| Leber, Theodor | <person> German ophthalmologist, 1840-1917. See: Leber's idiopathic stellate neuroretinitis, Leber's hereditary optic atrophy, Leber's plexus, amaurosis congenita of Leber. (05 Mar 2000) |
| amaurosis congenita of Leber | An autosomal recessive cone-rod abiotrophy causing blindness or severely reduced vision at birth. (05 Mar 2000) |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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레버마린정 - 새창
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신호제약 |
A15250491 | Carduus Marianus extract | 일반의약품 | 삭제 |
| 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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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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