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- myotonic dystrophy cataract 肌强直营养不良性白内障
- Objective To summarize the clinical characteristics of myotonic dystrophy (DM). 摘要目的总结强直性肌营养不良症(DM)的临床特点。
- We report a laboratory-confirmed pediatric case of congenital myotonic dystrophy (CMD) in Taiwan. 摘要我们报告一例台湾地区之先天型肌强直失状症的儿童个案。
- The SK3 channel was overexpressed in skeletal muscles after denervation and in patients with myotonic dystrophy(DM). 使去神经支配和肌强直营养不良患者骨骼肌SK3表达显著上调。
- Myotonic dystrophy is a degenerative disease characterized by progressive muscle wasting and weakness. 强直性肌营养不良是一种退行性疾病，以进展性肌肉萎缩和无力为特征。
- Objective To study the clinical and pathology features of myotonic dystrophy (DM). 摘要目的探讨强直性肌营养不良症(DM)的临床及肌肉病理学的特点。
- Cataract and myotonic dystrophy: the role of molecular diagnosis 强直性肌营养不良与白内障的分子诊断关系
- The conditions were familial adenomatous polyposis, myotonic dystrophy, multiple endocrine neoplasia, hereditary motor and sensory neuropathy. 这些疾病包括家族腺瘤息肉
- People with myotonic dystrophy have prolonged muscle tensing （myotonia） and are not able to relax certain muscles after use. 强直性肌营养不良病患具长期肌肉拉紧（肌强直）和在使用后无法放松某些肌肉。
- A disorder due to a similar molecular basis, myotonic dystrophy 1 (DM1), is known to have white matter hyperintensities on cranial MRI. 另一种有类似分子病理学基础的疾病：萎缩性肌强直(DM1)患者的核磁共振成像也有白质高信号。
- People with myotonic dystrophy have prolonged muscle tensing (myotonia) and are not able to relax certain muscles after use. 患有强直性肌营养不良者骨骼肌收缩为持续性收缩（强直），特定肌肉在使用后不能放松。
- Over time it became apparent that a central player in myotonic dystrophy was RNA, a versatile molecule that is very similar to DNA. 随着时间推移，很明显RNA在强直性肌营养不良中起了核心作用，RNA是一种类似于DNA普遍存在的分子。
- Patients with myotonic dystrophy, the most common form of adult-onset muscular dystrophy, have a high prevalence of insulin resistance due to disruption of the insulin receptor. 强直性肌营养不良是最常见的成年发病的肌营养不良症，由于胰岛素受体的破坏导致胰岛素抵抗的发病率很高。
- Objective To study the relationship between the changes of cytosine,thymine,guanine(CTG)repeat numbers and brain stem BAEP,SEP and VEP in patients with myotonic dystrophy(DM) and their family members. 目的探讨强直性肌营养不良(DM)患者及其家系成员三核苷酸重复数CTG(胞嘧啶、胸腺嘧啶、鸟嘌呤)的变化与脑干听觉诱发电位(BAEP)、体感诱发电位(SEP)、视觉诱发电位(VEP)的关系。
- Objective To study the relationship between the changes of cytosine，thymine，guanine（CTG）repeat numbers and brain stem BAEP,SEP and VEP in patients with myotonic dystrophy（DM） and their family members. 目的探讨强直性肌营养不良(DM)患者及其家系成员三核苷酸重复数CTG（胞嘧啶、胸腺嘧啶、鸟嘌呤）的变化与脑干听觉诱发电位(BAEP)、体感诱发电位(SEP)、视觉诱发电位(VEP)的关系。
- However, having established a general concept of what a treatment for myotonic dystrophy may look like, researchers believe that the next steps in developing an effective drug should go faster. 研究者建立了治疗强直性肌营养不良的概念，相信下一步开发一种有效的药物应该很快。
- Falls and stumbles in myotonic dystrophy 强直性肌营养不良患者的跌倒及绊倒
- Myotonic dystrophy with peripheral damage 伴有周围神经损害的强直性肌营养不良
- Clinical characteristics of myotonic dystrophy 强直性肌营养不良症的临床特点
- Keywords Myotonic dystrophy CTG ECG; 强直性肌营养不良;CTG;心电图;
