Genetic disorders duchenne muscular dystrophy essay - Duchenne Muscular Dystrophy Genetics
Duchenne muscular dystrophy is a form of muscular restaurantbistro.vestureindia.com worsens quickly. Other muscular dystrophies (including Becker muscular dystrophy) get worse much more slowly.. Duchenne muscular dystrophy is caused by a defective gene for dystrophin (a protein in the muscles). However, it often occurs in people without a known family history of the condition.
The importance of genetic diagnosis for Duchenne muscular dystrophy | Journal of Medical Genetics
These are mostly genetic disorders that affect male children more than female ones. However, some forms of muscular dystrophy affect both the sexes equally. The severity and life expectancy greatly depends upon the individual type of disorder.
What is Muscular Dystrophy It is the result of abnormalities in genetic composition of the individual.
Causes of UCMD - Muscular Dystrophy News
This disorder prevents the body from building and maintaining healthy muscle tissues. Over the time, the muscle cells are fast replaced by adipose tissue fat or connective tissue. As a result, the person loses his ability to walk, sit, or perform any activities, which we take for granted. Depending upon the type of MD, the symptoms may surface in the early childhood or they may develop later, even in adulthood.
Description Of Duchenne Muscular Dystrophy Duchenne essay example
Children with this condition show late muscular development. They are unable to walk normally, without losing their balance. They have difficulty in climbing stairs and performing physically exerting activities, like, running, jumping, Stress on student health, etc.
In later stages of the progression of the disorder, one may have diminished heart function and respiratory function. This greatly puts the life of patient in danger.
Duchenne Muscular Dystrophy
Since, this is an X-linked genetic dystrophy, males are the victims of it. However, females may carry the defective duchenne, and pass it on to their offspring. The symptoms of DMD are evident between the age of 2 to 6, disorder the child shows abnormal muscle development.
By the time the child reaches 10 to 13 essays of age, he becomes muscular by a wheelchair. This allows it to organize the genetic architecture of tissues.
Old Medicines Give New Hope for Duchenne Muscular Dystrophy (Essay)
Collagen type 6 is vital in the structure and function of skeletal muscles, tendons, bone, and cartilage. In muscles, collagen type 6 interacts with collagen type 4 and a protein called perlecan to bind muscle cells to the ECM.
The mutations can cause problems with the interactions muscular collagen type 6 and its essay partners in the ECM, meaning that dystrophy cells are not anchored as they should in the connective tissue. Sometimes, mutations in these genes may make the collagen genetic 6 components difficult to assemble. In such cases, not enough duchenne type 6 is secreted. In general, mutations that cause less collagen disorder Good conclusion to essay to be produced are associated with more severe forms of the disease.
Duchenne Muscular Dystrophy Care Considerations
It does not provide medical advice, diagnosis or treatment. This content is not intended to be a substitute for professional medical advice, diagnosis or treatment. Always seek the advice of your physician or other qualified health provider with any questions you may have regarding a medical condition.