myopathic

简明释义

英[maɪəˈpæθɪk]美[maɪəˈpæθɪk]

肌病的

英英释义

单词用法

同义词

反义词

例句

1.The spontaneous activities such as fibrillation and positive sharp wave could be observed when myopathic patients held their breath.

与对照者相比，肌病患者屏气时可见纤颤电位及正锐波等自发电位；

2.The spontaneous activities such as fibrillation and positive sharp wave could be observed when myopathic patients held their breath.

与对照者相比，肌病患者屏气时可见纤颤电位及正锐波等自发电位；

3.Physical therapy can help improve mobility in those with myopathic 肌病的 symptoms.

物理治疗可以帮助改善那些有myopathic 肌病的 症状的人的活动能力。

4.Research is ongoing to find effective treatments for myopathic 肌病的 conditions.

研究仍在进行中，以寻找有效的治疗myopathic 肌病的 状况的方法。

5.Some myopathic 肌病的 diseases are hereditary and can be passed down through generations.

一些myopathic 肌病的 疾病是遗传性的，可以通过几代人传递。

6.The patient was diagnosed with a myopathic 肌病的 condition that affected his muscle strength.

患者被诊断为一种影响肌肉力量的myopathic 肌病的 状况。

7.Doctors often use genetic testing to identify myopathic 肌病的 disorders in patients.

医生常常使用基因检测来识别患者的myopathic 肌病的 疾病。

作文

Myopathy is a term that refers to diseases that affect muscle tissue, leading to weakness and dysfunction. One particular aspect of myopathy that has garnered attention is its classification as a hereditary condition. Individuals who suffer from myopathic disorders often experience a gradual decline in muscle strength, which can significantly impact their quality of life. In this essay, I will explore the implications of myopathic conditions, their causes, and the importance of early diagnosis and intervention.The term myopathic encompasses a variety of muscle diseases, including muscular dystrophies and inflammatory myopathies. Muscular dystrophies are genetic disorders characterized by progressive muscle degeneration and weakness. On the other hand, inflammatory myopathies are caused by inflammation of the muscles, which can be triggered by autoimmune diseases or infections. Regardless of the specific type, all myopathic conditions share common symptoms such as muscle weakness, fatigue, and cramps.Understanding the causes of myopathic disorders is crucial for developing effective treatment strategies. Many myopathic conditions are inherited in an autosomal dominant or recessive manner, meaning they can be passed down from one generation to another. Genetic mutations play a significant role in the development of these disorders, with researchers identifying specific genes associated with various types of myopathy. For instance, mutations in the dystrophin gene lead to Duchenne muscular dystrophy, a severe form of muscular dystrophy that primarily affects boys.Early diagnosis of myopathic conditions is essential for managing symptoms and improving patient outcomes. Healthcare professionals often rely on a combination of clinical evaluations, genetic testing, and muscle biopsies to determine the presence of a myopathic disorder. Once diagnosed, patients may benefit from physical therapy, medications, and assistive devices to help maintain mobility and independence. Additionally, ongoing research into gene therapy and other innovative treatments holds promise for future advancements in the field of myopathy.Living with a myopathic condition can be challenging, both physically and emotionally. Patients often face limitations in their daily activities, which can lead to feelings of frustration and isolation. Support from family, friends, and healthcare providers is vital in helping individuals cope with the realities of their condition. Furthermore, raising awareness about myopathic disorders can foster a more supportive community and encourage research funding for better treatment options.In conclusion, myopathic disorders represent a significant challenge for those affected and their families. By understanding the nature of these conditions, their genetic underpinnings, and the importance of early intervention, we can work towards improving the lives of individuals living with myopathy. Ongoing research and increased awareness will be key in addressing the complexities of myopathic diseases and fostering a future where those affected can lead fulfilling lives.

肌病是指影响肌肉组织的疾病，导致肌肉无力和功能障碍。肌病的一个特殊方面引起了人们的关注，即它被归类为遗传性疾病。遭受肌病障碍的个体通常会经历肌肉力量的逐渐下降，这可能会显著影响他们的生活质量。在这篇文章中，我将探讨肌病状况的影响、其原因以及早期诊断和干预的重要性。术语肌病涵盖了多种肌肉疾病，包括肌营养不良症和炎症性肌病。肌营养不良症是一种遗传性疾病，以进行性肌肉退化和无力为特征。而炎症性肌病则是由肌肉的炎症引起的，这可能是由自身免疫疾病或感染引发的。无论具体类型如何，所有肌病状况都有共同的症状，如肌肉无力、疲劳和痉挛。理解肌病障碍的原因对于制定有效的治疗策略至关重要。许多肌病状况以常染色体显性或隐性方式遗传，这意味着它们可以从一代传递到另一代。基因突变在这些疾病的发展中起着重要作用，研究人员已确定与各种类型的肌病相关的特定基因。例如，肌萎缩性侧索硬化症中的dystrophin基因突变导致杜氏肌营养不良症，这是一种主要影响男孩的严重肌营养不良症。早期诊断肌病状况对管理症状和改善患者结果至关重要。医疗专业人员通常依赖临床评估、基因检测和肌肉活检的组合来确定是否存在肌病障碍。一旦确诊，患者可能会从物理治疗、药物和辅助设备中受益，以帮助维持活动能力和独立性。此外，对基因治疗和其他创新治疗的持续研究为肌病领域的未来进展带来了希望。与肌病状况生活可能是具有挑战性的，无论是身体上还是情感上。患者通常在日常活动中面临限制，这可能导致挫折感和孤立感。来自家人、朋友和医疗提供者的支持对于帮助个人应对其状况的现实至关重要。此外，提高对肌病障碍的认识可以促进更具支持性的社区，并鼓励对更好治疗选择的研究资金。总之，肌病障碍对受影响的人及其家庭构成了重大挑战。通过了解这些状况的性质、其遗传基础以及早期干预的重要性，我们可以努力改善生活在肌病中的个体的生活。持续的研究和增强的意识将是解决肌病疾病复杂性的关键，并促进受影响者过上充实生活的未来。