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

Authors

  • Abhishek Taklekar Graduate, Dr. DY Patil College of Physiotherapy, Pune.
  • Akhil Samson Assistant Professor, Dr. DY Patil College of Physiotherapy, DY Patil Vidyapeeth, Sant Tukaram Nagar, Plot No BGP/190Pimpri, Pune-411028. E-mail: akhil.samson@dpu.edu.in
  • Tushar Palekar Professor & Principal, Dr. DY Patil College of Physiotherapy, Pune.

DOI:

https://doi.org/10.15621/ijphy/2020/v7i4/750

Keywords:

Limb-girdle muscular dystrophy(LGMD), Miyoshi Myopathy, Dysferlinopathy, Quality of life, Structured exercise regimen, Aquatic therapy.

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.

References

Miyoshi K. Kawai H, Kusakuk I and Nishino H. Autosomal recessive distal muscular dystrophy as a new type of progressive muscular dystrophy. Seventeen cases in eight families including an autopsied case. Brain. 1986; 109:31-54.

Mishra UK, Kalita J. Clinical Neurophysiology. 3rd ed; 2013

Ropper, Allan H. Adams and Victor's Principles of Neurology. 10th ed; 2014

Distal Myopathy - NORD (National Organization for Rare Disorders]. NORD (National Organization for Rare Disorders). [cited 8th December 2019.] Available from: https://rarediseases.org/rare-diseases/distal-myopathy

M A. Dysferlinopathy. PubMed. 2020 [cited 4 December 2019]. Available from: https://www.ncbi.nlm.nih.gov/pubmed/20301480

Cárdenas A et al. Dysferlin function in skeletal muscle: Possible pathological mechanisms and therapeutical targets in dysferlinopathies. Expneurol. 2016; 283:246-254.

Biondi O et al. Dual Effects of Exercise in Dysferlinopathy. ASIP. 2013;182(6):2298-2309.

Urtizberea J, Bassez G, Leturcq F, Nguyen K, Krahn M, Levy N. Dysferlinopathies. Neurology India. 2008; 56(3):289.

Miyoshi myopathy | Genetic and Rare Diseases Information Center (GARD) – an NCATS Program. Rarediseases.info.nih.gov. 2019 [cited 13th December 2019] Available from: https://rarediseases.info.nih.gov/diseases/9676/miyoshi-myopathy

Takahashi, Keiichi. "Effects of Prednisone on a Patient with Dysferlinopathy Assessed by Maximal Voluntary Isometric Contraction: Alternate-Day Low-Dose Administration for a 17-Year Period." Case Rep Neurol.2019; 11(1): 10-16.

Patel N, Van Dyke K, Espinoza L. Limb-Girdle Muscular Dystrophy 2B and Miyoshi Presentations of Dysferlinopathy. AMJMS. 2017; 353(5):484-491.

ExRx.net : ACSM Indications For Termination of an Exercise Test [Internet]. Exrx.net. 2020 [cited 24 December 2019]. Available from: https://exrx.net/Testing/TestTermination

Aimee K, Kathleen M. Aquatic and Land-Based Physical Therapy Improves Functional Mobility and Quality of Life in a Patient with Bethlem Myopathy Muscular Dystrophy: A Case Report. JPPR. 2017; 02(01).

Saini M, Lorenzo N. Limb-Girdle Muscular Dystrophy Clinical Presentation: History, Causes. Emedicine.medscape.com. 2020 [cited 9 January 2020]. Available from: https://emedicine.medscape.com/article/1170911

Khadilkar, SatishV, et al. Limb-girdle muscular dystrophies in India: A review. Ann Indian Acad Neurol. 2017; 20(2): 87.

Sevinsky S. MMT Grading System. Scottsevinsky.com. 2020. [cited 15th January 2020]. Available from: http://www.scottsevinsky.com/pt/mmt.html

Published

09-08-2020
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How to Cite

Abhishek Taklekar, Akhil Samson, & Tushar Palekar. (2020). EFFECT OF STRUCTURED EXERCISE REGIMEN ON QUALITY OF LIFE, BALANCE AND STRENGTH ON A PATIENT WITH MIYOSHI MYOPATHY – A CASE REPORT. International Journal of Physiotherapy, 7(4), 186–191. https://doi.org/10.15621/ijphy/2020/v7i4/750

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Section

Case Study