先天性アンチトロンビン欠損症
WordNet
- present at birth but not necessarily hereditary; acquired during fetal development (同)inborn, innate
PrepTutorEJDIC
- 〈U〉〈C〉(…の)(量・額などの)不足,欠乏《+『of』(『in』)+『名』》 / 〈C〉不足分,不足量,不足額 / 〈C〉(精神・肉体などの)欠陥
- (病気・身体的欠陥など)生まれつきの,先天的な
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English Journal
- Initial diagnosis of the congenital disorder of glycosylation PMM2-CDG (CDG1a) in a 4-year-old girl after neurosurgical intervention for cerebral hemorrhage.
- Stefanits H1, Konstantopoulou V, Kuess M, Milenkovic I, Matula C.
- Journal of neurosurgery. Pediatrics.J Neurosurg Pediatr.2014 Nov;14(5):546-9. doi: 10.3171/2014.7.PEDS14102. Epub 2014 Sep 5.
- The congenital disorder of glycosylation characterized by a deficiency of phosphomannomutase 2 (PMM2-CDG) is the most common variant of congenital disorders of glycosylation. Besides typical clinical features, such as dysmorphism and abnormal body fat distribution, coagulation abnormities often lead
- PMID 25192236
- Clinical presentation and molecular basis of congenital antithrombin deficiency in children: a cohort study.
- Kumar R1, Chan AK, Dawson JE, Forman-Kay JD, Kahr WH, Williams S.
- British journal of haematology.Br J Haematol.2014 Jul;166(1):130-9. doi: 10.1111/bjh.12842. Epub 2014 Mar 29.
- In this study we report the largest descriptive cohort of congenital antithrombin (AT) deficiency in children, its clinical presentation, molecular basis and genotype-phenotype correlation. Paediatric patients diagnosed with AT deficiency at two tertiary care children's hospitals over a 10-year peri
- PMID 24684277
- Blood clots. Good when you're bleeding; bad when you're not bleeding hypercoagulability and thrombophilia--overview and case report.
- Cohen HV, Gurung S, Quek SY, Subramanian G, Abbas A.
- Journal of the New Jersey Dental Association.J N J Dent Assoc.2014 Summer;85(3):17-20.
- A critical and recurrent situation faced by the dental clinician (DC) is that of providing care to patients who may be at risk for excessive bleeding during care or post-operatively. Bleeding disorders may be due to congenital and/or acquired conditions affecting platelets and/or the coagulation pro
- PMID 25291832
Japanese Journal
- 若年発症の深部静脈血栓症に対して局所的血栓溶解療法が奏功した先天性アンチトロンビンⅢ(AT Ⅲ) 欠損症の1症例
- 細川 泰三,山中 俊明,川上 大志,清家 史靖,佐藤 澄子,山田 忠克,三根生 和明,岡山 英樹,風谷 幸男,中村 陽一
- 心臓 45(6), 713-720, 2013
- 組織プラスミノーゲン活性化因子(tissue plasminogen activator；tPA)は強力な血栓溶解薬である．深部静脈血栓に対してtPAの有用性が示唆されるが，出血などの合併症をきたし得る．今回，われわれは若年発症の深部静脈血栓症に対して局所的血栓溶解療法が奏功したアンチトロンビンⅢ(ATⅢ)欠損症の1症例を経験したので報告する．症例は19歳，男性．急激に右下肢の疼痛と歩行困難が出現 …
- NAID 130004688820
- SMV血栓による遅発性空腸狭窄を腹腔鏡下に切除した先天性AT-III欠損症の1例
- 岡 洋右,赤木 由人,衣笠 哲史,吉田 武史,白水 和雄
- 日本臨床外科学会雑誌 74(12), 3344-3349, 2013
- 症例は20歳，男性．上腹部痛と下痢・嘔吐認め受診した．CTにて上腸間膜静脈から門脈，右内外腸骨静脈から総腸骨静脈の血栓と，小腸の浮腫と拡張認めた．血液凝固線溶系検査にて先天性アンチトロンビンIII（以下，AT-III）欠損症と診断された．抗凝固療法とAT-III製剤投与にて血栓は消失し退院した．翌月，腹痛・嘔吐にて受診し，CTにて血栓の再発は認めなかったが，遅発性の空腸狭窄を認め，腹腔鏡補助下に小 …
- NAID 130004518575
- 深部静脈血栓症を有する先天性ATIII欠乏症を併存したS状結腸癌の1例
- 甲賀 淳史,岡本 和哉,奥村 拓也,山下 公裕,鈴木 憲次,川辺 昭浩
- 日本臨床外科学会雑誌 = The journal of the Japan Surgical Association 73(5), 1174-1179, 2012-05-25
- NAID 10030988691
Related Links
- Antithrombin III is a protein in the blood that blocks abnormal blood clots from forming. It helps the body keep a healthy balance between bleeding and clotting. Congenital antithrombin III deficiency is an inherited disease.
- Congenital antithrombin III deficiency is a genetic disorder that causes the blood to clot more than normal. ... A.D.A.M., Inc. is accredited by URAC, also known as the American Accreditation HealthCare Commission (www.urac.org
★リンクテーブル★
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- 英
- congenital antithrombin deficiency
- 関
- アンチトロンビン欠損症
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- 不足、欠乏、欠失、欠如、欠損、不十分。栄養不足、栄養素欠乏、欠乏症。(遺伝子)(染色体内の)遺伝子欠失
- 欠けているもの、不足している物。不足分。不完全なもの、欠点のあるもの
- 関
- absence, agenesis, dearth, defect, defective, deficient, deficit, delete, deletion, deletional, depletion, deprivation, deprive, lack, miss, missing, morphological defect, paucity, scarce, scarcity, starve
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- 関
- congenital、congenitally
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アンチトロンビン欠乏症
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アンチトロンビンIII