telangiectasia的意思

telangiectasia中文翻譯：

n.毛細管擴張（等于telangiectasis）

相似詞語短語

ataxia telangiectasia───運動失調性毛細血管擴張癥；路-巴二氏綜合征；共濟失調性毛細血管擴張癥；共濟失調毛細血管擴張癥

雙語使用場景

Irritable, angry telangiectasia, may cause skin redness, and sometimes result in rosacea.───急躁、生氣時毛細血管擴張，會引起皮膚發紅，有時也會造成酒渣鼻。

Objective to investigate the characteristics of the cytogenetic anomalies of ataxia telangiectasia.───目的探討共濟失調毛細血管擴張癥的細胞遺傳學異常特點。

The sun is like a stimulant, human exposure will telangiectasia, accelerate blood circulation.───而陽光猶如一種興奮劑，照射人體會使毛細血管擴張，加快血液循環。

To the best of our knowledge, brain capillary telangiectasia rarely has been previously reported by SWI.───就我們所知，腦內毛細血管擴張鮮少以磁敏感加權影像來報告。

Objective To localize the pathogenic gene of hereditary hemorrhagic telangiectasia (HHT) in a Chinese family of Han Nationality.───目的定位一個中國漢族遺傳性出血性毛細血管擴張癥家系的致病基因。

Capillary telangiectasia or transitional capillary-venous malformation was diagnosed.───診斷為毛細血管擴張或過渡型毛細血管-靜脈畸形。

The most common cause is dural pathology, in which a cavity lesion is associated with a small bleeding source such as a telangiectasia.───最常見的病因是硬腦（脊）膜病變，硬膜腔病變常伴有諸如毛細血管擴張之類的小出血灶。

Hereditary hemorrhagic telangiectasia (HHT) or Rendu-Osler-Weber disease (ROW) is a disorder that presents with recurrent episodes of EPX.───遺傳性毛細血管擴張癥（HHT）或Rendu-Osler-Weberdisease（ROW）是一種表現為反復出血發作的障礙。

英語使用場景

Niton can improve skin telangiectasia and has good curative effect on nerves, arthritis, gynecopathy and barrenness. It is a good beauty agent and it also has good rejuvenation effect for men.

Causing telangiectasia, permeability, smooth muscle spasm, glandular secretion and so on.

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

BACKGROUND AND STUDY AIMS: Hereditary hemorrhagic telangiectasia (HHT) is a rare autosomal dominant disorder characterized by telangiectasia formation that can lead to small-bowel bleeding.

Furthermore, idiopathic telangiectasia (spider-like veins) and varicose veins will also reduce or even completely prevent, reduce the risk of thrombosis or embolism.

To the best of our knowledge, brain capillary telangiectasia rarely has been previously reported by SWI.

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.

Capillary telangiectasia or transitional capillary-venous malformation was diagnosed.

Irritable, angry telangiectasia, may cause skin redness, and sometimes result in rosacea.