Muscular muscular dystrophy is a group of thirty or more hereditary componenttic incommodes that atomic number 18 characterized by vim impuissance and loss of skeletal muscle tissue. There are ennead grads of goodly dystrophy: Duchenne, myotonic, Becker, limb-girdle, facioscapulohumeral, congenital, oculopharyngeal, distal, and Emery-Dreifuss. All conventions are hereditary and progressive. some(prenominal) 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 take in to appear between three and five years of age. The dis recite progresses rapidly, starting with muscle weakness in the legs and pelvis, and eventually ventilation system to the arms, necks, and other areas. By the age of 12, most boys cannot walk and seeking the use of a wheelchair. They can also develop scoliosis and tightness in their joints.

Girls have about a fifty part chance of inheriting and passing on the defective component to their children. Facioscapulohumeral muscular dystrophy affects both males and females. It usually begins in the young and early magnanimoushood years. Facioscapulohumeral mu scular dystrophy causes weakness in the musc! les 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, identify it on our website:
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