EFFECT OF STRUCTURED EXERCISE REGIMEN ON QUALITY OF LIFE, BALANCE AND STRENGTH ON A PATIENT WITH MIYOSHI MYOPATHY – A CASE REPORT

IF 0.1 Q4 ORTHOPEDICS International Journal of Physiotherapy Pub Date : 2020-08-01 DOI:10.15621/ijphy/2020/v7i4/750
Abhishek Taklekar, Akhil Samson, T. Palekar
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引用次数: 1

Abstract

Background: Dysferlinopathy is an autosomal recessive disease seen in adolescence or young adulthood. Miyoshi Myopathy is characterized by weakness and wasting of posterior compartment leg muscles rather than the anterior compartment and distal upper limb muscles. Still, the intrinsic muscles of the foot and hands are spared. There are several undiagnosed cases in India and also around the world with dysferlinopathy. Diagnosis for the same requires advanced biological laboratories along with high economic funding for diagnostic purposes. Case Summary: This case report presents a 22-year-old male diagnosed with Miyoshi myopathy/LGMD2b (dysferlinopathy). The subject complained about a loss of balance, strength, and difficulty in performing activities of daily living. The patient was given Aquatic Therapy along with conventional physical therapy for a duration of 6weeks, which included three days of supervised therapy along with 3days home protocol and a rest day kept at the end of every week. Outcome Measures: Standardized scales like the Barthel Index and the Berg Balance Scale were used for the assessment of pre and post the progress of the subject for Quality of Life and Balance, respectively. Manual Muscle testing was used for assessments for pre and post muscle strength of the subject. Conclusion: The timely diagnosis of a rare condition before the advancement of the disorder and thus the use of appropriate intervention of physiotherapy, which consisted of progressive muscle-strengthening exercises along with balance training proved to be promising in preventing falls, muscle atrophy and thus making the patient independent for doing daily activities.
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有组织的运动方案对生活质量的影响,平衡和力量对三良肌病患者-一个病例报告
背景:异ferlinopathy是一种常染色体隐性遗传病,常见于青春期或青年期。三好肌病的特征是小腿后腔室肌肉无力和萎缩,而不是前室和上肢远端肌肉。尽管如此,脚和手的内在肌肉却没有受到影响。在印度和世界各地都有一些未确诊的异ferlinopathy病例。诊断同样需要先进的生物实验室以及用于诊断目的的高经济资金。病例总结:这一病例报告提出了一个22岁的男性诊断为三吉肌病/LGMD2b(异ferlinopathy)。患者自诉失去平衡、力量,难以进行日常生活活动。患者在接受常规物理治疗的同时接受水中疗法,为期6周,其中包括3天的监督治疗和3天的家庭治疗,每周结束休息一天。结果测量:Barthel指数和Berg平衡量表等标准化量表分别用于评估受试者在生活质量和平衡方面的前后进展。手工肌肉测试用于评估受试者前后的肌肉力量。结论:在疾病进展前及时诊断出罕见的疾病,并采用适当的物理治疗干预,包括渐进式肌肉强化训练和平衡训练,在预防跌倒和肌肉萎缩方面有希望,从而使患者能够独立进行日常活动。
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