WordNet

any bundle of nerve fibers running to various organs and tissues of the body (同)nervus
optical properties; "the optics of a telescope"
the branch of physics that studies the physical properties of light
control of your emotions; "this kind of tension is not good for my nerves"

PrepTutorEJDIC

〈C〉『神経』 / 〈C〉《複数形で》『神経過敏』,いらだち / 〈U〉『勇気』,度胸(courage) / 〈U〉《時にa ~》厚かましさ,ずぶとさ;無礼 / 〈C〉葉脈;(昆虫の)翅脈(しみゃく) / 〈人,特に自分〉‘に'力を与える,‘を'元気づける
光学
(・・・を)選ぶ《+『for』+『名』》;(・・・するほうを)選ぶ《+『to』 do》
目の;視覚の

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1. 視神経の先天性および後天性異常 congenital anomalies and acquired abnormalities of the optic nerve
2. 原発性乳児緑内障 primary infantile glaucoma
3. 白色瞳孔を有する小児に対するアプローチ approach to the child with leukocoria
4. 鼻の先天異常 congenital anomalies of the nose
5. 腎発育不全 renal hypoplasia

Rahimy E1, Rahimy E2.
Ophthalmology.Ophthalmology.2016 May;123(5):990. doi: 10.1016/j.ophtha.2016.02.039.
PMID 27107352

Retinal ischaemia and delayed fibrovascular proliferation associated with an optic nerve coloboma.

Pastora N1, Peralta J2, Abelairas J2.
Archivos de la Sociedad Espanola de Oftalmologia.Arch Soc Esp Oftalmol.2016 Apr;91(4):184-187. doi: 10.1016/j.oftal.2015.12.013. Epub 2016 Feb 3.
CASE REPORT: A patient with a left optic nerve coloboma with late development (at 15 years of age) of vitreoretinal fibrovascular proliferation and tractional retinal detachment (TRD). Sectorial retinal photocoagulation was performed with regression of the proliferative tissue and exudation.DISCUSSI
PMID 26850327

Familial Disorders of the Optic Disc: Presentation of a Mother and Daughter and Review of the Literature.

Hsu CL1, Layton CJ2.
Case reports in ophthalmology.Case Rep Ophthalmol.2015 Jul 29;6(2):251-9. doi: 10.1159/000437381.
Optic disc pit and optic nerve coloboma are examples of congenital optic disc abnormalities. Although optic nerve coloboma can be inherited in an autosomal dominant fashion, no conclusive link has been found in the case of optic disc pit as an autosomal dominant disease. We describe two cases: a dau
PMID 26327911

中野万智子,柳田英彦,杉本圭相,藤田真輔,岡田満,竹村司
日本小児腎臓病学会雑誌 = Japanese journal of pediatric nephrology 21(2), 212-216, 2008-11-15
　今回われわれは，新規のPAX2遺伝子異常を有し，精神発育遅滞を伴った腎コロボーマ症候群の1例を経験した。13歳時に，すでに軽度な腎機能低下と中等度の蛋白尿を認めていた。腎生検では，メサンギウム基質の増加と糸球体虚脱，糸球体周囲の繊維化，尿細管基底膜の肥厚や萎縮，間質の細胞浸潤と繊維化を認め，腎コロボーマ症候群に合致する所見であった。両眼ともにコロボーマを認めた。PAX2遺伝子解析を実施したところ …
NAID 10025170595