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MUSCULAR DYSTROPHY CURE BY - - COMPLETE, PERMANENT , EASY, SAFE , FAST & COSTEFFECTIVE PERMANENT MODERN HOMOEOPATHY CURE Muscular dystrophy (MD) is a group of inherited diseases in which the muscles that control movement (called voluntary muscles) progressively weaken. In some forms of this disease, the heart and other organs are also affected. Muscular dystrophy can appear in infancy up to middle age or later, and its form and severity are determined in part by the age at which it occurs. Some types of muscular dystrophy affect only males; some people with MD enjoy a normal life span with mild symptoms that progress very slowly; others experience swift and severe muscleweakness and wasting, dying in their late teens to early 20s. Muscular dystrophy (MD) is a group of muscle diseases that results in increasing weakening and breakdown of skeletal muscles over time.[1] The disorders differ in which muscles are primarily affected, the degree of weakness, how fast they worsen, and when symptoms begin.[1] Many people will eventually become unable to walk. Some types are also associated with problems in other organs.[2][not in citation given] There are nine main categories of muscular dystrophy that contain more than thirty specific types.[1][2] The most common type is Duchenne muscular dystrophy (DMD) which typically affects males beginning around the age of four. Other types include Becker muscular dystrophy, facioscapulohumeral muscular dystrophy, and myotonic dystrophy.[1] They are due to mutations in genes that are involved in making muscle proteins. This can occur due to either inheriting the defect from one's parents or the mutation occurring during early development. Disorders may be X-linked recessive, autosomal recessive, or autosomal dominant. Diagnosis often involves blood tests and genetic testing.[2] There is no cure for muscular dystrophy. Physical therapy, braces, and corrective surgery may help with some symptoms.[1] Assisted ventilation may be required in those with weakness of breathing muscles.[2] Medications used include steroids to slow muscle degeneration, anticonvulsants to control seizures and some muscle activity, and immunosuppressants to delay damage to dying muscle cells. Outcomes depend on the specific type of disorder.[1] Duchenne muscular dystrophy, which represents about half of all cases of muscular dystrophy, affects about one in 5, 000 males at birth. Muscular dystrophy was first described in the 1830s by Charles Bell. The word "dystrophy" is from the Greek dys, meaning "difficult" and troph meaning "nourish". Gene therapy, as a treatment, is in the early stages of study in humans.[2] DR ARPIT CHOPRA (MD HOMOEOPATHY) Chief Consultant Homoeopath & Biochemic AAROGYA SUPERSPECIALITY MODERN HOMOEOPATHIC CLINIC(Computerised) 102, First Floor, Krishna Tower, Opposite Curewell Hospital, Newpalasia, Indore (M.P.) Mob 9713092737 / 9713037737/ 9907527914(whats up no) PH - 0731-2532737, 3961737 website- www.homoeopathycure.com