Journals / Gümüşhane Üniversitesi Sağlık Bilimleri Dergisi / 2022 / Cilt: 11 - Sayı: 4

Duchenne Muscular Dystrophy and Electrical Stimulation

Duchenne Musküler Distrofi ve Elektrik Stimülasyonu

Pages
1644–1653
Publication Date
2022-12-22
DOI
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

The purpose of this review is to bring together studies on DMD and electrical stimulation.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Duchenne Muscular Dystrophy (DMD) is an X-linked recessive genetic disease with a prevalence of approximately 1/3600-6000 live in male births.
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Key Findings & Data:It is the most common type of muscular dystrophy in childhood and characterized by progressive muscle weakness.
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Conclusion & Impact:The purpose of this review is to bring together studies on DMD and electrical stimulation.
🔬Design:Review & Systematic Survey
📍Scope:Comprehensive Sample
⚙️Variables:Duchenne Muskuler Distrofi · Nöromusküler Hastalık · Elektirik Stimülasyonu

Abstract

Duchenne Muscular Dystrophy (DMD) is an X-linked recessive genetic disease with a prevalence of approximately 1/3600-6000 live in male births. It is the most common type of muscular dystrophy in childhood and characterized by progressive muscle weakness. DMD mainly affects boys, women are just genetic carriers and they are usually asymptomatic or have mild symptoms. Although a great deal of progress has been made with current clinical studies on treatment, no method that completely cures the disease has yet been reported. Electrical stimulation is used within the scope of physiotherapy and rehabilitation programs in neuromuscular diseases, but there are few studies and different opinions in the literature about the presence of genetic defects and fatigue, and disinsection that may occur after the applications. The purpose of this review is to bring together studies on DMD and electrical stimulation.

Özet

Duchenne Musküler Distrofi (DMD), X kromozomuna bağlı resesif geçiş gösteren ve yaklaşık 1/3600-6000 canlı erkek doğum prevelansı olan genetik bir hastalıktır. DMD esas olarak erkek çocukları etkileyen, ilerleyici kas zayıflığı ile karakterize, kadınların taşıyıcı olup genellikle asemptomatik veya hafif belirti gösterdiği çocukluk çağında en sık görülen musküler distrofi tipidir. Tedavi konusunda günümüzde güncel klinik araştırmalar ile büyük bir yol kat edilmiş olsa da hastalığı tamamen tedavi eden herhangi bir yöntem henüz bildirilmemiştir. Nöromusküler hastalıklarda fizyoterapi ve rehabilitasyon programı kapsamında elektrik stimülasyonu kullanılmaktadır fakat genetik defektin varlığı ve uygulamalar sonrası oluşabilecek yorgunluk ve dejenerasyon konusunda literatürde az sayıda çalışma ve farklı görüşler bulunmaktadır. Bu derlemenin amacı DMD ve elektrik stimülasyonuyla ilgili yapılan çalışmaları bir araya getirmektir.

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Cite This Article

YENER, B., ALIKMA, A. F., GÜNDÜZ, D., ZEREN, H., KURBAN, K., AKDIKAN, M., ALPASLAN, S. N., ÖZGÜL, S., SALDIRAN, T. Ç. (2022). Duchenne Muscular Dystrophy and Electrical Stimulation. Gümüşhane Üniversitesi Sağlık Bilimleri Dergisi, Cilt: 11 - Sayı: 4, 1644–1653. https://ajindex.com/articles/859596

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References (1)

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