Optic Atrophy, Hereditary, Leber : KMLE 의학 검색 엔진 - 의학사전, 의학용어, 의학약어, 의학논문, 약품/의약품 검색

MeSH(Medical Subject Headings) 맞춤 검색 (http://www.nlm.nih.gov) 결과 : 1 페이지: 1

Optic Atrophy, Hereditary, Leber - 새창 A maternally linked genetic disorder that presents in mid-life as acute or subacute central vision loss leading to central scotoma and blindness. The disease has been associated with missense mutations in the mtDNA, in genes for Complex I, III, and IV polypeptides, that can act autonomously or in association with each other to cause the disease. (from Online Mendelian Inheritance in Man, http://www.ncbi.nlm.nih.gov/Omim/, MIM#535000 (April 17, 2001))
Synonyms : Leber Hereditary Optic Neuropathy, Leber Optic Atrophy, Leber's Hereditary Optic Atrophy, Leber's Hereditary Optic Neuropathy, Leber's Optic Atrophy, Optic Atrophy, Leber, Hereditary, Lebers Optic Atrophy, Optic Atrophy, Leber, Optic Atrophy, Leber's