Muscular dystrophy is a group of thirty or more hereditary componenttic incommodes that ar characterized by vim flunk and loss of skeletal muscle tissue. There are ennead chance variables of goodly dystrophy: Duchenne, myotonic, Becker, limb-girdle, facioscapulohumeral, congenital, oculopharyngeal, distal, and Emery-Dreifuss. All diversitys are hereditary and progressive. whatsoever of the symptoms include progressive muscular wasting, poor respite and coordination, unfitness to walk, scoliosis, drooping eyelids, and respiratory difficulty. There is currently no be restored 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 use up to appear between three and five years of age. The dis name progresses rapidly, starting with muscle weakness in the legs and pelvis, and eventually breathing to the arms, necks, and other areas. By the age of 12, most boys cannot walk and interest the use of a wheelchair. They can also develop scoliosis and constriction in their joints. Girls have about a fifty percent chance of inheriting and passing on the defective gene 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 abnormal ities, and endocrine disturbances. Those aff! ected by myotonic muscular...If you want to get a full essay, place it on our website: OrderCustomPaper.com
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