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Muscular dystrophy

Muscular dystrophy (abbreviated MD) refers to a group of hereditary muscle diseases that weakens the muscles that move the human body. Muscular dystrophies are characterized by progressive skeletal muscle weakness, defects in muscle proteins, and the death of muscle cells and tissue.

Nine diseases including Duchenne, Becker, limb girdle, congenital, facioscapulohumeral, myotonic, oculopharyngeal, distal, and Emery-Dreifuss are always classified as muscular dystrophy but there are more than 100 diseases in total with similarities to muscular dystrophy. Most types of Muscular dystrophy are multi-system disorders with manifestations in body systems including the heart, gastrointestinal and nervous systems, endocrine glands, skin, eyes and even brain.

The Major Forms of MD

  • Becker muscular dystrophy (BMD): Affects older boys and young men. Causes progressive muscle weakness, usually beginning in the legs. It is similar to Duchenne muscular dystrophy, but is generally milder.
  • Congenital muscular dystrophy (CMD): A rare form present from birth. Symptoms usually progress slowly and include general weakness, flaccid tone, bent joints, and slow motor development. Fukuyama CMD is another type of congenital CMD that usually involves mental retardation.
  • Facioscapulohumeral muscular dystrophy (FSH): Also known as Landouzy-Dejerine disease. Begins in late childhood to early adulthood. Affects both males and females. Causes weakness in the muscles of the face, shoulders, and upper arms. May also affect the hips and legs.
  • Limb-girdle muscular dystrophy (LGMD): Starts in late childhood to early adulthood. Affects males and females. Causes weakness in the muscles around the upper legs and shoulders.
  • Myotonic dystrophy: Also known as Steinert's disease. Symptoms may begin any time from birth through adulthood. Affects males and females. Generalized weakness first occurs in the face, hands, and feet. People with this disease also have myotonia, the failure of the muscles to relax normally after use.
  • Distal muscular dystrophy (DD): Symptoms begin in middle age or later. Causes weakness in the muscles of the feet and hands.
  • Duchenne muscular dystrophy (DMD): The most severe form. Affects young boys. Causes progressive muscle weakness, usually beginning in the legs.
  • Emery-Dreifuss muscular dystrophy (EDMD): Affects young boys. Causes muscle contractions in the calves; weakness in the calves, shoulders, and upper arms; and problems in the way electrical impulses travel through the heart to make it beat.
  • Oculopharyngeal muscular dystrophy (OPMD): Affects adults of both sexes. Causes weakness in the eye muscles and throat.

Muscular dystrophy can affect people of all ages. Although some forms first become apparent in infancy or childhood, others might not appear until middle age or later. Duchenne muscular dystrophy (DMD) is the most common form affecting children, while myotonic MD is the most common form affecting adults.The accumulation of toxins of vata types particularly weakens the mamsha dhatu and makes one susceptible to MD
Treatment
MD has no cure till date in modern system of medicines only symptomatic treatments are available and research continues.
This condition have similar pathogenesis effecting mamsha dhatu & some types of Avaranas is treatable in view of Maharishi Charaka. Taking leads from the authentic source we at Vedanta Ayurveda Centre India worked in the area & developed a unique approach in selecting ayurveda based herbal concentrates based on the state & nature of disease & diseased person in convenient dosages form & are found very effective in MD in more than 60% of the cases in improving the muscles strenght of the patients & the effects usually starts after 45days of course of personalized herbal food supplements.

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