Pragmatic Neurorehabilitation Approach for Improving Quality of Life in Duchenne Muscular Dystrophy: A Case Report
Radha Nangliya, Anam R Sasun, Snehal Samal

TL;DR
This case report shows how physiotherapy can improve quality of life for a child with Duchenne muscular dystrophy.
Contribution
The study demonstrates a six-week physiotherapy program's effectiveness in managing DMD symptoms and improving patient outcomes.
Findings
The patient showed significant improvement in outcome measures after six weeks of physiotherapy.
Physiotherapy strategies included diet management, stretching, splinting, and pulmonary training.
Multidisciplinary care is crucial for managing DMD symptoms and complications.
Abstract
This case report provides insights into the physiotherapy management of a 12-year-old male with Duchenne muscular dystrophy (DMD). DMD is a devastating genetic disorder characterized by progressive muscle degeneration and weakness. Skeletal muscle degeneration is induced by a genetic disorder. It is a common X-linked condition that causes hypertrophy of the calves and proximal muscular weakness in children. It frequently results in early mortality, wheelchair confinement, and delays in motor development. Physiotherapy interventions aim to optimize functional abilities and quality of life in individuals with DMD. This case report highlights the effectiveness of physiotherapy in managing DMD progression. This study presents a case exhibiting notable clinical symptoms, highlighting the urgency for advanced treatments to combat this debilitating disease. Outcome measures such as body mass…
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Taxonomy
TopicsMuscle Physiology and Disorders · Neurogenetic and Muscular Disorders Research · Children's Physical and Motor Development
