Muscular dystrophy is a group of thirty or more hereditary componenttic incommodes that argon characterized by vim impuissance and loss of skeletal muscle tissue. There are night club word hurls of goodly dystrophy: Duchenne, myotonic, Becker, limb-girdle, facioscapulohumeral, congenital, oculopharyngeal, distal, and Emery-Dreifuss. All forms are hereditary and progressive. more or less of the symptoms include progressive muscular wasting, poor respite and coordination, softness to walk, scoliosis, drooping eyelids, and respiratory difficulty. There is currently no bring back for any form of muscular dystrophy. The symptoms of muscular dystrophy are treatable with medications, physical therapy, and surgery. The most common form of muscular dystrophy is Duchenne. Duchenne muscular dystrophy primarily affects boys. It is caused by the absence of dystrophin, a protein involved in maintaining the integrity of muscle. Symptoms usually let trim to appear between three and five years of age. The dis sort progresses rapidly, starting with muscle weakness in the legs and pelvis, and eventually airing to the arms, necks, and other areas. By the age of 12, most boys cannot walk and pick up the use of a wheelchair. They can also develop scoliosis and tightness in their joints.

Girls have about a fifty percentage chance of inheriting and passing on the defective divisor to their children. Facioscapulohumeral muscular dystrophy affects both males and females. It usually begins in the teenage and early magnanimoushood years. Facioscapulohumeral muscular dystrophy causes weakness in the muscles of the face, arms, legs, and ! shoulders and chest. This form of muscular dystrophy progresses slowly. Symptoms may range from meek to severe. myotonic muscular dystrophy affects males and females. This is the most common adult form and symptoms may begin any time from fork up to childhood. It is characterized by muscle spasms, cataracts, cardiac abnormalities, and endocrine disturbances. Those affected by myotonic muscular...If you want to get a full essay, lodge it on our website:
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