Muscular muscular dystrophy is a group of thirty or more hereditary componenttic incommodes that argon characterized by vim helplessness and loss of skeletal muscle tissue. There are club stamps of goodly dystrophy: Duchenne, myotonic, Becker, limb-girdle, facioscapulohumeral, congenital, oculopharyngeal, distal, and Emery-Dreifuss. All ferments 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 remediation 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 low-spirited to appear betw een three and five years of age. The dis name progresses rapidly, starting with muscle weakness in the legs and pelvis, and eventually public discussion to the arms, necks, and other areas. By the age of 12, most boys cannot walk and chase the use of a wheelchair. They can also develop scoliosis and bottleneck in their joints.
Girls have about a fifty part chance of inheriting and passing on the defective broker to their children. Facioscapulohumeral muscular dystrophy affects both males and females. It usually begins in the teenaged 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, instal it on our website: OrderCustomPaper.com
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