telangiectasia中文,telangiectasia的意思,telangiectasia翻译及用法

2025-11-01 20:43 浏览次数 9

telangiectasia

英[telˌændʒɪˌek'teɪʒə]美[telˌændʒɪˌek'teɪʒə]

n. 毛细管扩张(等于telangiectasis)

telangiectasia 英语释义

英语释义

    1. an abnormal dilation of red, blue, or purple superficial capillaries, arterioles, or venules typically localized just below the skin's surface (as of the face) — compare spider vein

    2. an abnormal dilation of red, blue, or purple superficial capillaries, arterioles, or venules typically located just below the skin's surface (as on the face) — see ataxia-telangiectasia, hereditary hemorrhagic telangiectasia, spider vein

telangiectasia 片语

片语

hereditory telangiectasia遗传性毛细血管扩张癥

conjunctival telangiectasia结膜毛细管扩张

verrucosa telangiectasia翻译

hemorrhagic telangiectasia出血性毛细血管扩张癥

spider telangiectasia蜘蛛痣

essential telangiectasia翻译

gastric telangiectasia胃毛细血管扩张

palpebral telangiectasia睑毛细管扩张

lymphatica telangiectasia翻译

telangiectasia 例句

英汉例句

  • Hereditary hemorrhagic telangiectasia (HHT) or Rendu-Osler-Weber disease (ROW) is a disorder that presents with recurrent episodes of EPX.

    遗传性毛细血管扩张癥(HHT)或Rendu - Osler - Weberdisease (ROW)是一种表现为反复出血发作的障碍。

  • Methods a retrospective review was conducted of 133 patients with telangiectasia treated with VPW532 laser.

    方法:使用VPW532激光治疗毛细血管扩张133例,观察其疗效和不良反应。

  • Objective: To study the treatment of nosebleed caused by hereditary hemorrhagic telangiectasia (HHT).

    目的:探讨遗传性出血性毛细血管扩张癥所引起鼻出血的治疗方法。

  • Hereditary hemorrhagic telangiectasia is an uncommon autosomal dominant inheritance disease. 25 cases from a family were reported. The pathology, clinical presentation and treatment were discussed.

    遗传出血性毛细血管扩张癥为常染色体显性遗传病,临床少见,本文就其病理变化、临床特点进行讨论,探讨其治疗方法。附一家系25例分析。

  • Specific evaluations: Pain in ribs, tongue demonstration, hepatauxe, enlarged spleen, spider telangiectasia in liver palm.

    具体评价内容:胁肋疼痛、舌象、肝肿大、脾肿大、肝掌蜘蛛痣。

  • Mutations in the corresponding ATM gene result in ataxia telangiectasia (at), an autosomal recessive disease characterized by uncoordinated muscle movement and neurodegeneration.

    AT M基因突变可导致共济失调毛细血管扩张癥(AT),一种常染色体隐性遗传病,该病特点是不协调的肌肉运动和神经退化。

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