Muscular Dystrophy :: essays research papers

Discovered in 1861 by Guillaume B.A. Duchenne, powerful sizeable dystrophy is a really unfortunate disease to inherit. Muscular dystrophy is a throng of heredity disorders characterized by progressive muscle weakness and wasting. The trait for herculean dystrophy may be transmitted as an autosomal dominant. In this case, if any(prenominal) original carrier of the disease had children, the children would have a equal chance of inheriting the disease. It is also carried as an autosomal recessive trait, in which case the offspring of the original carrier would have a truly small chance of inheriting the trait. Muscular dystrophy is also a sex-linked trait. If well-nighone carrying the trait for the disease conceived a male, the newborn male child would have a very high risk of later on developing the disease. Incidence of muscle dystrophy is estimated to be one in 3-4,000 male births. there ar also about 15,000 respectable dystrophy patients in the United States at any giv en time. Those who have muscular dystrophy atomic number 18 absentminded the protein called ?dystrophin.? Before scientists ever discovered the absent protein, the tested carriers for the disease had a high presence of elevated serum levels of creatine and phosphokinase. The disease can now be found for a prenatal diagnosis. Individuals who inherit this disease will have a fast progression of symptoms. Walking becomes difficult, and skeletal contractures and muscle atrophy follows. They also ordinarily need wheelchairs by adolescence. Half of the receivers of the disease unfortunately develop some form of mental retardation and most never make it historical there teenage years. Currently, options for a treatment of muscular dystrophy are limited. Physical therapy may slow down the progression of deformities. Such devices as wheel chairs, crutches, or secondary orthopedic limbs may permit mobility. in that location are also a few medications that can help lighten pain and stif fness in the muscles. The Muscular Dystrophy Association, the Parent suggest Muscular Dystrophy Research and the Childrens Hospital of Pittsburgh helped fund a question project for the disease. The look, carried out by Johnny Huard, Ph.Muscular Dystrophy essays search papersDiscovered in 1861 by Guillaume B.A. Duchenne, muscular dystrophy is a very unfortunate disease to inherit. Muscular dystrophy is a conference 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 recessive 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 trait for the disease conceived a male, th e newborn male child would have a very high risk of later 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 discovered the missing protein, the tested carriers for the disease had a high presence of elevated serum levels of creatine and phosphokinase. The disease can now be found 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 make it former(prenominal) there teenage years. Currently, options for a treatment of muscular dystrophy are limited . Physical therapy may slow down the progression of deformities. Such devices as wheel chairs, crutches, or secondary orthopedic limbs may permit mobility. There are also a few medications that can help buy up pain and stiffness in the muscles. The Muscular Dystrophy Association, the Parent thrust 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.