An Ayurvedic Perspective About Duchenne Muscular Dystrophy

Ashwini A. Patil, Rutuja Rahul Kate
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Abstract

Duchenne muscular dystrophy is a neuromuscular disease. This is an X-linked recessive disease caused by mutations in the dystrophin protein gene located on the short arm of the X chromosome, in the Xp21 region. It causes progressive muscle weakness due to wasting of muscle fibers. It causes loss of ability to stand, walk, and move before age 10; most patients die in their 20s. Since there is no specific treatment in any medical system and the prognosis of the disease is uncertain, if we start treatment at an early stage, children with DMD can walk, it can slow or stop progressive muscle degeneration. DMD cannot be directly related to a single disease in Ayurveda. Most major neuromuscular disorders are determined by Vata dosha. In Ayurveda, this pathogenesis can be clearly understood by the concept of Adibala Pravrutta Vyadhi (genetic disease). Here the pathogenesis is due to Beeja Bhagavayava Dusti (partial chromosomal defect) leading to Mamsa Vata Dushti.
关于杜兴氏肌肉萎缩症的阿育吠陀观点
杜氏肌营养不良症是一种神经肌肉疾病。这是一种 X 连锁隐性遗传病,由位于 X 染色体短臂 Xp21 区域的肌营养蛋白基因突变引起。由于肌纤维萎缩,它会导致进行性肌无力。这种病会导致患者在 10 岁前丧失站立、行走和移动的能力;大多数患者在 20 多岁时死亡。由于目前尚无特效治疗方法,该病的预后也不确定,但如果我们在早期就开始治疗,DMD 患儿就可以行走,可以减缓或阻止进行性肌肉退化。在阿育吠陀中,DMD 无法与单一疾病直接相关。大多数主要的神经肌肉疾病都是由瓦塔体质(Vata dosha)决定的。在阿育吠陀中,"Adibala Pravrutta Vyadhi"(遗传病)的概念可以清楚地解释这种发病机制。这里的发病机制是由于 Beeja Bhagavayava Dusti(部分染色体缺陷)导致 Mamsa Vata Dushti。
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