Common "Muscular Dystrophy" queries answered by top doctors | iCliniq

Muscular Dystrophy

Muscular dystrophy includes several progressive muscle diseases that cause progressive weakness and muscle wastage leading to loss of muscle mass. There are more than 30 types of such dystrophy. The most common type is Duchenne muscular dystrophy. In addition, Becker, myotonic, congenital, limb-girdle, facioscapulohumeral, distal, oculopharyngeal, Emery-Dreifuss are some other types. Improper balance, waddling gait, large calf muscles, muscle wastage, scoliosis, walking disability, etc., are the symptoms. These are rare muscle disorders and are due to genetic predisposition. These are due to the genetic mutation of the muscle-making protein. Although there is no cure, the symptoms can be slowed down with various therapies and medication.

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All the answers published on this website are written by verified Native and Traditional Care Experts. The Content has been moderated by the iCliniq Content Review Team before publication. Post your health questions on iCliniq-Native Care by choosing the right Native Care Specialty and get them answered. Your queries will be answered 24/7 by top Native Care Experts from iCliniq-Native Care.

My 2 year old son has Duchenne Muscular Dystrophy. Will he walk?

Query: Hello doctor,My youngest son is 2 and a half years old. Currently, he is crawling, and he is delayed in walking. I bought him for the child development clinic at the hospital. They have sent his blood sample to another country, and the result says that he has Duchenne Muscular Dystrophy. Kindly advi...  Read Full »


Dr. Alka

Answer: Hello, Welcome to icliniq.com. It is a genetic disorder. I am sorry to say this, as this disease has a poor prognosis. You need to visit a medical genetic specialist. Physical therapy, braces, etc. are common management. Along with that if you want to go for alternative treatment, then try Ayurved...  Read Full »

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