WordNet

located at or near or behind a part or near the end of a structure

PrepTutorEJDIC

《名詞の前にのみ用いて》(生物学的に,位置が)後ろの,後部の / (時間・順序が)後の;(…より)後の《+『to』+『名』》(later) / しり(buttocks)

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1. 新生児胆汁うっ滞の原因 causes of neonatal cholestasis
2. 経膣メッシュ曝露と骨盤手術後の疼痛のマネージメント management of transvaginal mesh exposure and pain following pelvic surgery
3. Reversible cerebral vasoconstriction syndromes
4. 膣後壁欠損の外科的マネージメント surgical management of posterior vaginal defects
5. 成人における選択的脊椎手術のための麻酔 anesthesia for elective spine surgery in adults

English Journal

Discordant clinical phenotype in monozygotic twins with Alagille syndrome: Possible influence of non-genetic factors.

Izumi K1,2, Hayashi D1, Grochowski CM3, Kubota N4,5, Nishi E1,5,6, Arakawa M1, Hiroma T7, Hatata T8, Ogiso Y9, Nakamura T5,7, Falsey AM3, Hidaka E4,5, Spinner NB3,10.
American journal of medical genetics. Part A.Am J Med Genet A.2016 Feb;170(2):471-5. doi: 10.1002/ajmg.a.37429. Epub 2015 Oct 13.
Alagille syndrome is a multisystem developmental disorder characterized by bile duct paucity, congenital heart disease, vertebral anomalies, posterior embryotoxon, and characteristic facial features. Alagille syndrome is typically the result of germline mutations in JAG1 or NOTCH2 and is one of seve
PMID 26463753

Alagille's syndrome associated with proximal radio-ulnar synostosis: Clinical case and a literature review.

Couceiro J1, Gómez B2, Sanmartín M3.
Revista espanola de cirugia ortopedica y traumatologia.Rev Esp Cir Ortop Traumatol.2016 Jan-Feb;60(1):81-85. doi: 10.1016/j.recot.2014.05.007. Epub 2014 Jul 16.
Alagille's syndrome is an infrequent genetic condition with autosomal inheritance and variable expression. The complete form exhibits 5 clinical signs, chronic intrahepatic cholestasis, characteristic facies, cardiovascular anomalies, posterior embryotoxon, and vertebral defects. If only 3 or 4 of t
PMID 25037110

The frequency of occurrence of certain corneal conditions by age and sex in Iranian adults.

Hashemi H1, Khabazkhoob M1, Emamian MH2, Shariati M3, Yekta A4, Fotouhi A5.
Contact lens & anterior eye : the journal of the British Contact Lens Association.Cont Lens Anterior Eye.2015 Dec;38(6):451-5. doi: 10.1016/j.clae.2015.05.005. Epub 2015 Jun 2.
PURPOSE: To determine the prevalence of posterior embryotoxon, corneal opacity, pigment on endothelium, corneal dystrophy, and corneal vascularization in a middle-aged Iranian population, and their association with age and sex.METHODS: In a cross-sectional study with multistage cluster sampling, sub
PMID 26044921

Japanese Journal

Axenfeld-Rieger 症候群に対するトラベクロトミー時に発見されたシュレム管の位置異常について

岩城正佳,三宅豪一郎,片岡卓也,永田徹也,菅敬文,雑喉正泰,竹内篤
日本眼科紀要 = Folia ophthalmologica Japonica 56(1), 40-44, 2005-01-28
NAID 10017250089

Clinical Evaluation of Posterior Embryotoxon in One Institution

OZEKI Hironori,SHIRAI Shoichiro,MAJIMA Akio,SANO Masahiro,IKEDA Kozo
Japanese journal of ophthalmology 41(6), 422-425, 1997-11-01
NAID 10018023107

A Case of Rieger's Syndrome with Leg Length Discrepancy.

中村英一,水田博志,白石稔,高木克公,久保田健治
整形外科と災害外科 45(4), 1241-1244, 1996
… She had Rieger's anomaly characterized by posterior embryotoxon, hypoplasia of the anterior leaf of the iris and strands bridging over the iridocorneal angle associated with hydroceplalus, flat nasal root, sensory deafness, mitral insufficiency, shortening of her left lower extremity. …
NAID 130001630998

Related Pictures

Slit-lamp examination revealed posterior embryotoxon, iris hypoplasia, | Download Image result for posterior embryotoxon alagille syndrome bryan's blog: My eye abnormalities - part 1 Posterior embryotoxon (arrowed). Courtesy of Mr Anthony Quinn. | Download Scientific anteriorcleavagesyndrome Posterior embryotoxon - American Academy of Ophthalmology Fuse, Mol Vis 2007; 13:1005-1009. Figure 1. Axenfeld-Rieger syndrome