athetosis词根词缀

Results In the 6 unrelated families of PD patients, 1 case had exon 5 deletion, its hereditary manner was autosomal recessive inheritance, the patient's age at the onset was 60 years old, clinical feature was tremor, rigidity and bradykinesia, but no athetosis.

结果6例患者中，发现1例有第5外显子缺失，其遗传模式呈常染色体隐性遗传，起病年龄60岁，临床表现为震颤、僵直和运动迟缓，但无异动症。

Methods: 50 children patients have been chosen who were diagnosed at clinic or in sickroom from Nov. 2005 to Mar. 2006. They have been divided into three groups: hemiplegia, athetosis and the others.

方法：收集2005年11月～2006年3月在大连市儿童医院康复门诊就诊或住院的50例脑瘫患儿作为研究对象，分为偏瘫型、手足徐动型和其它型。

All of the patients who had parkin gene deletion mutation had tremor, rigidity and bradykinesia, but athetosis and family history of PD were not found.

所有缺失突变病例均有震颤、僵直和运动迟缓，但无异动症和PD家族史；