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1)  Pseudo-Budd-Chiari syndrome
假性Budd-Chiari综合征
1.
Pseudo-Budd-Chiari syndrome usually occurs in patients with alcoholic liver disease, and its sonographic and radiographic findings were similar to that of Budd-Chiari syndrome.
假性Budd-Chiari综合征多发生于酒精性肝病的患者,其彩超和CT检查类似于Budd-Chiari综合征,而选择性下腔静脉造影无异常发现。
2)  Budd-Chiari syndrome
Budd-Chiari综合征
1.
The diagnostic value of color doppler sonography in the diagnosis of Budd-Chiari syndrome;
彩色多普勒超声对Budd-Chiari综合征的诊断价值
2.
Discrimination between Budd-Chiari Syndrome,Hepatic Veno Occlusive Disease and Liver Cirrhosis;
Budd-Chiari综合征、肝小静脉闭塞病与肝硬化的鉴别
3.
Clinical study on percutaneous transhepatic angioplasty of hepatic veins in treatment of Budd-Chiari syndrome with occlusion of hepatic veins;
经皮肝穿刺肝静脉成形术治疗肝静脉阻塞型Budd-Chiari综合征的临床研究
3)  Budd-Chiari Syndrone
Budd-Chiari氏综合征
4)  BUDD CHIARI SYNAROME/surg
BUDD-CHIARI综合征/外科学
5)  Osteoporosis pseudoglioma syndrome
骨质疏松假性神经性胶质瘤综合征
6)  opsteoporosis pseudoglioma syndrome
骨质疏松-假性神经胶质瘤综合征
补充资料:假性软骨发育不全性椎骺发育不良综合征


假性软骨发育不全性椎骺发育不良综合征


该综合征为常染色体显性遗传。表现:出生后生长不良,肢体短,至2岁最明显,成人时身高82~130cm。步态蹒跚。干骺端不规则,蘑菇状。骨骺小,不规则,尤其股骨头骺。骨干短,弓形,以下肢为著。椎骨不同程度扁平,前方舌形,椎根短,腰椎前挺,后凸,侧弯。肋骨有匙状倾向。除肘以外,其他大关节过度活动。智力正常。出生后外观正常,即能区别于真正的软骨发育不全。
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