修复毛细血管扩张，美白补水。
Repair the expansion of capillary vessels, whitening and water-supplement.
探讨小肠毛细血管扩张症的诊断和治疗方法。
To explore the diagnosis and therapeutic methods of small intestinal telangiectasis.
目的探讨共济失调毛细血管扩张症的细胞遗传学异常特点。
Objective to investigate the characteristics of the cytogenetic anomalies of ataxia telangiectasia.
发红是毛细血管扩张造成的，尤其是那些拥有敏感皮肤的人。
Redness is caused by a dilation of the capillaries, especially in those with sensitive skin.
方法：回顾分析一例颅内（广泛）毛细血管扩张症的DSA表现。
Method Retrospective study and analysis of DSA presentations of cerebral extensive telangiectasis in 1 case.
半数病人可并发遗传性毛细血管扩张症，还可并发脑梗塞和脑脓肿。
About half of the patients supervene telangiectasis, and also associated with cerebral infarction and brain abscess.
目的：探讨遗传性出血性毛细血管扩张症所引起鼻出血的治疗方法。
Objective: To study the treatment of nosebleed caused by hereditary hemorrhagic telangiectasia (HHT).
或是疤痕样表面光滑的纤维样斑，无明显毛细血管扩张、溃疡及隆起。
Or it is the fiber appearance spot with scar shape smooth face without dilate of apparent blood capillary ulcer and apophysis.
在皮肤，结果将是气温升高的真皮，毛细血管扩张，并刺激血液循环。
In skin, the result will be elevated dermis temperature, expanded blood capillaries, and stimulated blood circulation.
或是疤痕样表面光滑的纤维样斑，无明显毛细血管扩张、溃疡及隆起。
Or it is the fiber appearance spot with scar shape smooth face, without dilate of apparent blood capillary, ulcer and apophysis.
毛细血管扩张把更多氧气送入肌肉中并带走排泄物，如二氧化碳和乳酸。
Your small blood vessels (capillaries) will widen to deliver more oxygen to your muscles and carry away waste products, such as carbon dioxide and lactic acid.
激光处理对于婴儿血管瘤消失后，残留的毛细血管扩张的消退有效果。
Laser therapy is effective for fading telangiectasias that often remain after an infantile hemangioma has involuted.
急躁、生气时毛细血管扩张，会引起皮肤发红，有时也会造成酒渣鼻。
Irritable, angry telangiectasia, may cause skin redness, and sometimes result in rosacea.
而阳光犹如一种兴奋剂，照射人体会使毛细血管扩张，加快血液循环。
The sun is like a stimulant, human exposure will telangiectasia, accelerate blood circulation.
小腿出现许多象牙白色萎缩性瘢痕，伴毛细血管扩张、色素沉着、溃疡。
The patient presented with ivory white scars, telangiectasis, hyperpigmentation and ulcerations on the both lower legs.
方法结合我院近期收治的3例小肠毛细血管扩张症患者的临床资料进行分析。
Methods Clinical data of 3 cases with intestinal telangiectasis treated recently in our hospital were reviewed.
目的：探讨IPL对面部色斑、毛细血管扩张及皮肤衰老的治疗效果及影响因素。
Objective To explore the curative effect and the effective factor of IPL in treating face splash capillarectasia and skin consenescence.
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。
Methods a retrospective review was conducted of 133 patients with telangiectasia treated with VPW532 laser.
病程 3 月组，上述改变加重，毛细血管扩张、基底膜增厚，视杆细胞核固缩、异染色质浓集；
In 3-month-course group, all the changes above appeared to be more serious with capillarectasia, basement membrane thickened, rod-cell nucleus pyknosis and metachromatin condensed.
当你用磁铁来治疗损伤时可能要比用冰箱中的冰强十倍，它可使损伤附近的毛细血管扩张，致使损伤加速恢复。
When treated with magnets about 10 times stronger than the ones on your fridge, tiny blood vessels near an injury dilate, allowing for faster healing.
AT M基因突变可导致共济失调毛细血管扩张症(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。
Mutations in the corresponding ATM gene result in ataxia telangiectasia (at), an autosomal recessive disease characterized by uncoordinated muscle movement and neurodegeneration.
其中，蜘蛛状毛细血管扩张症23例，酒渣鼻6例，外用激素或化妆品后毛细血管扩张症34例以及局限性特发性毛细血管扩张症5例。
Out of 68 cases, 23 cases were spider telangiectasis, 6 cases were Rosacea, 34 cases were telangiectasis caused by steroids or cosmetics, and 5 cases were localized essential telangiectasis.
遗传出血性毛细血管扩张症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。
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.
根据我们的经验，对有症状的HHT相关毛细血管扩张症者，使用微粒进行的栓塞治疗提供了令人满意的即时止血效果，其疗效可维持3周到两年。
In symptomatic HHT-related telangiectasias, embolization with particles gives a satisfactory immediate result with immediate hemostasis, lasting from 3 weeks to 2 years in our experience.
遗传性毛细血管扩张症(HHT)或Rendu - Osler - Weberdisease (ROW)是一种表现为反复出血发作的障碍。
Hereditary hemorrhagic telangiectasia (HHT) or Rendu-Osler-Weber disease (ROW) is a disorder that presents with recurrent episodes of EPX.
过敏性休克时心肌收缩力减弱，小血管扩张，毛细血管通透性增加。
When allergic shock the cardiac muscle shrinkage force is weaken, the minute vessel expands, the blood capillary permeability increases.
过敏性休克时心肌收缩力减弱，小血管扩张，毛细血管通透性增加。
When allergic shock the cardiac muscle shrinkage force is weaken, the minute vessel expands, the blood capillary permeability increases.
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