Muscular Dystrophy :: essays research papers

Discovered in 1861 by Guillaume B.A. Duchenne, powerful fibrous muscular muscular dystrophy is a very unfortunate disease to inherit. Muscular dystrophy is a group of heredity disorders characterized by progressive muscle weakness and wasting. The distinction for muscular dystrophy may be transmitted as an autosomal dominant. In this case, if some original carrier of the disease had children, the children would cod a fifty-fifty chance of inheriting the disease. It is likewise carried as an autosomal recessionary trait, in which case the offspring of the original carrier would wear a very small chance of inheriting the trait. Muscular dystrophy is alike a sex-linked trait. If some matchless carrying the trait for the disease conceived a male, the newborn baby baby boy would have a very high risk of afterwards on break uping the disease. Incidence of muscle dystrophy is estimated to be single in 3-4,000 male births. There are overly about 15,000 muscular dystrophy pa tients in the United States at any given time. Those who have muscular dystrophy are missing the protein called ?dystrophin.? Before scientists ever find the missing protein, the tested carriers for the disease had a high presence of luxurious serum levels of creatine and phosphokinase. The disease can now be lay down for a prenatal diagnosis. Individuals who inherit this disease will have a rapid progression of symptoms. Walking becomes difficult, and skeletal contractures and muscle atrophy follows. They similarly usually need wheelchairs by adolescence. Half of the receivers of the disease unfortunately generate some form of mental retardation and most never bother it past there teenage years. Currently, options for a treatment of muscular dystrophy are limited. Physical therapy may slow down the progression of deformities. such(prenominal) devices as wheel chairs, crutches, or secondary orthopedic limbs may bear mobility. There are also a few medications that can dish re lieve pain and stiffness in the muscles. The Muscular muscular dystrophy Association, the kindle Project Muscular Dystrophy Research and the Childrens Hospital of Pittsburgh table serviceed fund a research project for the disease. The research, carried out by Johnny Huard, Ph.Muscular Dystrophy essays research papersDiscovered in 1861 by Guillaume B.A. Duchenne, muscular dystrophy is a very unfortunate disease to inherit. Muscular dystrophy is a group of heredity disorders characterized by progressive muscle weakness and wasting. The trait for muscular dystrophy may be transmitted as an autosomal dominant. In this case, if some original carrier of the disease had children, the children would have a fifty-fifty chance of inheriting the disease. It is also carried as an autosomal recessionary trait, in which case the offspring of the original carrier would have a very small chance of inheriting the trait. Muscular dystrophy is also a sex-linked trait. If someone carrying the tra it for the disease conceived a male, the newborn boy would have a very high risk of by and by on developing the disease. Incidence of muscle dystrophy is estimated to be one in 3-4,000 male births. There are also about 15,000 muscular dystrophy patients in the United States at any given time. Those who have muscular dystrophy are missing the protein called ?dystrophin.? Before scientists ever sight the missing protein, the tested carriers for the disease had a high presence of upgrade serum levels of creatine and phosphokinase. The disease can now be open up for a prenatal diagnosis. Individuals who inherit this disease will have a rapid progression of symptoms. Walking becomes difficult, and skeletal contractures and muscle atrophy follows. They also usually need wheelchairs by adolescence. Half of the receivers of the disease unfortunately develop some form of mental retardation and most never chance on it past there teenage years. Currently, options for a treatment of muscul ar dystrophy are limited. Physical therapy may slow down the progression of deformities. such(prenominal) devices as wheel chairs, crutches, or secondary orthopedic limbs may set aside mobility. There are also a few medications that can help relieve pain and stiffness in the muscles. The Muscular Dystrophy Association, the kick upstairs Project Muscular Dystrophy Research and the Childrens Hospital of Pittsburgh helped fund a research project for the disease. The research, carried out by Johnny Huard, Ph.