OPT : KMLE 의학 검색 엔진 - 의학사전, 의학용어, 의학약어, 의학논문, 약품/의약품 검색

MeSH(Medical Subject Headings) 맞춤 검색 (http://www.nlm.nih.gov) 결과 : 5 페이지: 1

Optic Atrophies, Hereditary - 새창 Hereditary conditions that feature progressive visual loss in association with optic atrophy. Relatively common forms include autosomal dominant optic atrophy (OPTIC ATROPHY, AUTOSOMAL DOMINANT) and Leber hereditary optic atrophy (OPTIC ATROPHY, HEREDITARY, LEBER).
Synonyms : Optic Atrophy, Hereditary, Atrophies, Hereditary Optic, Atrophy, Hereditary Optic, Hereditary Optic Atrophies
Optic Atrophy - 새창 Atrophy of the optic disk which may be congenital or acquired. This condition indicates a deficiency in the number of nerve fibers which arise in the RETINA and converge to form the OPTIC DISK; OPTIC NERVE; OPTIC CHIASM; and optic tracts. GLAUCOMA; ISCHEMIA; inflammation, a chronic elevation of intracranial pressure, toxins, optic nerve compression, and inherited conditions (see OPTIC ATROPHIES, HEREDITARY) are relatively common causes of this condition.
Synonyms : Atrophy, Optic
Optic Atrophy, Autosomal Dominant - 새창 Dominant optic atrophy is a hereditary optic neuropathy causing decreased visual acuity, color vision deficits, a centrocecal scotoma, and optic nerve pallor (Hum. Genet. 1998; 102: 79-86). Mutations leading to this condition have been mapped to the OPA1 gene at chromosome 3q28-q29. OPA1 codes for a dynamin-related GTPase that localizes to mitochondria.
Synonyms : Autosomal Dominant Optic Atrophy, Optic Atrophy Type 1, Optic Atrophy, Kjer Type, Dominant Optic Atrophies, Optic Atrophies, Dominant, Optic Atrophy, Dominant
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
Optic Chiasm - 새창 The X-shaped structure formed by the meeting of the two optic nerves. At the optic chiasm the fibers from the medial part of each retina cross to project to the other side of the brain while the lateral retinal fibers continue on the same side. As a result each half of the brain receives information about the contralateral visual field from both eyes.
Synonyms : Optic Chiasma, Optic Decussation, Chiasm, Optic, Chiasma Opticums, Chiasma, Optic, Chiasmas, Optic, Chiasms, Optic, Decussation, Optic, Decussations, Optic, Optic Chiasmas, Optic Chiasms, Optic Decussations, Opticum, Chiasma, Opticums, Chiasma