Diseaseless Program - Muscular Dystrophy
The definition of muscular dystrophy is atrophy or muscle weakness.
The muscular dystrophies (MD) refers to a group of genetic diseases characterized by progressive weakness and by the destruction of the muscle to the bone that controls movement.
The muscular dystrophy type many, others will notice from birth and congenital muscular dystrophy known as or just coming to birth of the baby and the others appear at the beginning of puberty (BECKER MD). Whatever the period of infancy, the other muscular dystrophy leads to injury or movement in paralysis
The three most common types of MD are: Duchenne, facioscapulohumeral, and myotonic. The three differ in the way of inheritance, time of commencement, the level of growth, and spread of disability. Ken Drew & Dr. Patel - Diseaseless Program
Onset is between 3 to 5 years old and spreads quickly. The majority of men will not walk in the 12th year of age, and at the age of 20 are required to use a respirator to breathe.
The myotonic MD differs what age begin to attack and known as myotonia (prolonged erection or pagpulikat of muscle) in the fingers and the muscles in the face: pagkalupaypay pagkalambot or feet, high-stepping walk; cataracts; heart disease; and endocrine unusual circumstances. People with myotonic is oblong shaped face and drooping eyelids; and the hair in front of the men
There is no specific antidote to either differing forms of MD. The physical terapyutikang usually done to avoid the painful twisting of the muscles
Some proposed medications can be used to manage the disease as well to curb the deterioration of the muscles in different types of MD. Read Our Privacy Policy Here
Orthopedic equipment is available to support and orthopedic surgery to correct the injury may be required to improve the quality of life of others. In other cases, the terapyutika breathing may be required, as mentioned previously. With the last hulian, heart disease may need the electronic instruments nagpapatibok heart or pacemaker.