angioedema

1. One case report of nerve angioedema associated with transient abdominal pain and ascites
   以突发突止腹痛、腹水为表现的神经血管性水肿1例报告
2. The primary end point was the number of attacks of angioedema per period, with each subject acting as his or her own control.
   最初终点为每周期血管性水肿发作数，由受试者自行控制。
3. In the past, angioedema was referred to by the term angioneurotic edema, which wrongly implied that the phenomenon was due to neurosis.
   在过去，血管被称为一词血管神经性水肿，这错误的暗示，这种现象是由于神经症。
4. History of angioedema with other DPP-4 inhibitors.
   血管性水肿的历史与其他DPP-4抑制剂。
5. Another case was considered to be anaphylaxis with symptoms of urticaria, angioedema, laryngeal edema, and palpitations, and the third case was considered to be a hoarse voice.
   另外一位过敏患者表现为荨麻疹，血管性水肿，喉头水肿和心悸，第三位女孩则是声音嘶哑。
6. Ten are for rare or "orphan" diseases, which frequently lack any therapy because of the small number of patients with the condition, such as a treatment for hereditary angioedema;
   十种药是为罕见或“孤儿”病，因为患者少的情况经常缺乏任何治疗，例如遗传性血管水肿治疗。
7. It showed that the most common form among them was exanthematous type, secondly were fixed eruption and urticaria angioedema types.
   发疹型药疹最为常见，其次为固定性红斑和荨麻疹与血管性水肿。
8. Lacidipine-induced acute urticaria and angioedema
   拉西地平致急性荨麻疹伴血管性水肿
9. Molecular Genetics Progress of Hereditary Angioedema
   遗传性血管性水肿分子遗传学进展
10. To identify the mutation of C1 inhibitor ( C1 INH) gene in a Chinese family with hereditary angioedema ( HAE).
    目的对一个遗传性血管水肿（HAE）家系患者C1抑制物（C1INH）基因的突变类型进行检测分析。
11. Hereditary angioedema ( HAE) is characterized by an inherited defect of C1 inhibitor ( C1INH).
    C1抑制物的遗传缺陷是遗传性血管性水肿（HAE）的基本特征。
12. Identification of a Novel Mutation of C1 Inhibitor Gene ina Chinese Family with Hereditary Angioedema
    一个遗传性血管水肿家系C1抑制物基因突变的检测分析
13. Soft tissue cervicofacial emphysema after dental treatment: Report of 2 cases with emphasis on the differential diagnosis of angioedema
    牙科治疗后面颈部软组织气肿：2例报道并强调与血管性水肿相鉴别
14. Hereditary angioedema ( HAE) is an autosomal dominant genetic disease caused by synthesis defect or dysfunction of C1 esterase inhibitor.
    遗传性血管性水肿是一种由于C1酯酶抑制剂的合成障碍或功能缺陷所致的常染色体显性遗传病。
15. Life-threatening orolingual angioedema during thrombolysis in acute ischemic stroke
    急性缺血性卒中患者溶栓期出现危及生命的口舌部血管性水肿
16. Hereditary angioedema is a rare autosomal dominant genodermatosis caused by C1 inhibitor ( C1 INH) gene mutations.
    遗传性血管性水肿是由C1酯酶抑制剂基因突变所致的一种罕见的常染色体显性遗传性疾病。
17. Chronic urticaria is a common skin disease, manifested by recurrent erythema, wheal with itching ( may be combined with angioedema), sustained at least six weeks.
    慢性荨麻疹（CU）是一类常见的皮肤病，表现为反复出现的红斑、风团伴瘙痒（可合并血管性水肿），持续至少六周以上。

noun

1. recurrent large circumscribed areas of subcutaneous edema

   Synonym:    atrophedemagiant hivesperiodic edemaQuincke's edema