C1酯酶抑制剂缺乏症的英文名字是C1 esterase inhibitor deficiency。基因解码表明:C1酯酶抑制剂缺乏症是由基因突变引起的。这种疾病是由于C1酯酶抑制剂的基因突变导致其功能受损或缺乏,从而影响了正常的免疫系统功能。这种基因突变可以是遗传的,也可以是后天发生的。
C1 esterase inhibitorcomplementgene therapyhereditary angioedemavascular permeabilityBackground Hereditary angioedema (HAE) is a life‐threatening, autosomal dominant disorder characterized by unpredictable, episodic swelling of the face, upper airway, oropharynx, extremities, genitalia, and gastrointestinal tract....
C1 esterase inhibitor protein is reduced to 10-30% of normal in patients with angioedema secondary to C1 esterase inhibitor deficiency (85% of patients with Hereditary Angioedema (HAE)); in 15% of patients with HAE, the concentrations of the inhibitor protein is normal but function is markedly...
(redirected from C1-esterase inhibitor deficiency)Also found in: Dictionary, Medical, Encyclopedia. Graphic Thesaurus 🔍 Display ON Animation ON Legend Synonym Antonym Related </>embed</> oedemahydropsedemadropsyQuincke's edemaperiodic edemagiant hivesatrophedemaangioedema noun Synonyms for angioe...
C1 Esterase Inhibitor, Human Plasma 英文名称: C1 Esterase Inhibitor, Human Plasma 总访问: 351 国产/进口: 进口 半年访问: 48 产地/品牌: Athens 产品类别: 分子生物学试剂 规格: 16-16-031509 最后更新: 2024-12-5 货号: CAS 号: 参考报价: 询价 立即询价 电话咨询 ...
Acquired C1 esterase inhibitor deficiency is a clinical syndrome closely resembling hereditary angioedema in which most patients have an associated malignancy of B cell lineage. Sera from 33 patients with B cell neoplasms were assayed for C1 esterase inhibitor level by rocket immunoelectrophoresis. The ...
中华内科杂志1989年第28卷第7期 C抑制物缺乏症‘ 北直 跣主巷反直辩 张誉 c抑制物映乏癌(c inhibitor 一’。。一 组罕见病 共特点是C;抑制蜘tC inhibitor— C.INH)量或质的缺乏,鉴于C。INH柱雏内昀重要椎 用,许骞国家已将此病列为重点研究课题 C:抑制物以前称C酯酶抑制物(c esteraseinhibi。 tot)...
and genitalia. Hereditary angioedema due to C1 esterase inhibitor deficiency is comprised of two clinically indistinguishable forms. In hereditary angioedema type 1, serum levels of C1 esterase inhibitor are decreased, while in type 2, the levels are normal or elevated, but the protein is non-funct...
Hereditary angioedema (HAE) is a rare autosomal dominant disease due to C1 esterase inhibitor deficiency (C1-INH). The disease is characterized by subcutaneous and submucosal edema in the absence of urticaria due to the accumulation of bradykinin. This descriptive study aimed to evaluate the clinical...
Acquired C1 esterase inhibitor deficiency A case of acquired C 1 esterase inhibitor deficiency and its anaesthetic implications is presented. Prophylaxis against angioneurotic oedema using danazol... PA Razis,IH Coulson,TR Gould,... - 《Anaesthesia》 被引量: 67发表: 2010年 The Janus faces of ac...