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.
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).
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.
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.
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.
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