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《所有・所属》…『の』,…のものである,…に属する・《材料・要素》…『でできた』,から成る・《部分》…『の』[『中の』] ・《数量・単位・種類を表す名詞に付いて》…の・《原因・動機》…『で』,のために(because of) ・《主格関係》…『の』,による,によって・《目的格関係》…『を』,の・《同格関係》…『という』・《関係・関連》…『についての』[『の』],の点で・《抽象名詞などと共に》…の[性質をもつ] ・《『It is』+『形』+『of』+『名』+『to』 doの形で,ofの後の名詞を意味上の主語として》・《分離》…『から』・《起原・出所》…『から』[『の』](out of) ・《『名』+『of』+『a』(『an』)+『名』の形で》…のような・《『名』+『of』+『mine』(『yours, his』など独立所有格)の形で》…の…・《時》(1)《副詞句を作って》…に《形容詞句を作って》…の・《時刻》《米》…前(to,《米》before)
(特定の事に関する,または特殊の性質の)文書資料の集成 / (研究用に収集した)資料
OLD French古[代]フランス語

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1. 神経管欠損および脳室拡大を除く中枢神経系異常の出生前診断 prenatal diagnosis of cns anomalies other than neural tube defects and ventriculomegaly
2. 視神経の先天性および後天性異常 congenital anomalies and acquired abnormalities of the optic nerve
3. 水頭症 hydrocephalus
4. 先天性奇形に対するアプローチ approach to congenital malformations
5. 神経管欠損症の超音波診断 ultrasound diagnosis of neural tube defects

Two cases of Vici syndrome associated with Idiopathic Thrombocytopenic Purpura (ITP) with a review of the literature.

Huenerberg K1, Hudspeth M2, Bergmann S2, Pai S3, Singh B3, Duong A1.
American journal of medical genetics. Part A.Am J Med Genet A.2016 May;170(5):1343-6. doi: 10.1002/ajmg.a.37589. Epub 2016 Feb 7.
Vici syndrome is a rare congenital disorder first described in 1988. To date, 31 cases have been reported in the literature. The characteristic features of this syndrome include: agenesis of the corpus callosum, albinism, cardiomyopathy, variable immunodeficiency, cataracts, and myopathy. We report
PMID 26854214

Breik O1, Mahindu A2, Moore MH3, Molloy CJ2, Santoreneos S2, David DJ3.
Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery.Childs Nerv Syst.2016 May;32(5):833-8. doi: 10.1007/s00381-016-3036-z. Epub 2016 Feb 10.
PURPOSE: Apert syndrome characterized by acrocephalosyndactyly is a rare autosomal dominant congenital malformation with a prevalence of 1/65,000 births. With an extensive range of phenotypic and developmental manifestations, its management requires a multidisciplinary approach. A variety of craniof
PMID 26861132

Al-Hashim AH1,2, Blaser S3, Raybaud C3, MacGregor D1.
Developmental medicine and child neurology.Dev Med Child Neurol.2016 May;58(5):475-84. doi: 10.1111/dmcn.12978. Epub 2015 Dec 9.
AIM: To study neuroradiological features in pediatric patients with corpus callosum abnormalities, using new functional subtyping for the corpus callosum, and to correlate the features with the clinical presentation.METHOD: We performed a retrospective review of 125 patients with radiologically iden
PMID 26661037