Essay on duchenne muscular dystrophy

The special education teacher and the physical and occupational therapists work with him closely to support his educational, physical, and unctional needs in all possible ways.

Since males only have one X-chromosome, if they inherit a gene for a disease present on the X, it will be expressed. This enlargement is a sign of muscle disease rather than an indication of good strength. Duchenne muscular dystrophy is Essay on duchenne muscular dystrophy to one out of every three thousand six hundred male infants due to this disease being inherited Essay on duchenne muscular dystrophy family members.

Women who are carriers of an X-linked disorder have a fifty-percent risk of transmitting the carrier condition to their daughters, and a fifty-percent risk of transmitting the disease to their sons. Accommodations for Academics The student with will need to be seated in the front of the class and with a peer buddy to accommodate them.

Current level of performance The student who is a 13 year old male is a very enthusiastic and happy boy who loves to read, be around people, and listen to music. Free essays on Health posted on this site were donated by anonymous users and are provided for informational use only.

Weakness progresses rapidly after age eight or nine, resulting in the inability to walk or stand alone. This test is one of the newest and most significant tests of technique.

An EMG test involves putting Cornehl 8 a small needle through the skin into a muscle and recording the pattern of electricity in the muscle when it is contracting. Use of a wheelchair proceeds from occasional use at about age nine years to almost total dependence by the early teens.

It seems to be important in maintaining the shape and structure of the muscle fiber. In the late stages of Duchenne muscular dystrophy, there is a noticeable shortening of muscles and the loss of muscle tissue.

Duchenne Muscular Dystrophy Essay Sample

Without dystrophin, Duchenne muscular dystrophy occurs. People often wonder how you know if you have Duchenne muscular dystrophy. Duchenne muscular dystrophy is more effective to those who have a family history of this miserable disease.

Dystrophin is a large protein, which is found on the inner side of the membrane surrounding each muscle fiber. Some cases may be mild and very slowly progressive, with normal lifespan, while other cases may have more marked progression of muscle weakness, functional disability and a loss of ambulation.

If parents have brought their son to a doctor at a very early stage of the disease, it may be difficult or impossible to detect anything definitely wrong on observing him.

On average, a diagnosis is not made until the child is five, although with increasing awareness of the problem, some boys are diagnosed earlier. A complete nervous system test may be run on the person with the signs of this disease. During the first few years, muscle fibers that break down in boys with Duchenne muscular dystrophy are being replaced, but the body has only a limit to continue replacing muscle fiber.

Duchenne muscular dystrophy is a rare neuromuscular disorder that is inherited as an X-linked recessive trait. When women who have male kids have a fifty percent chance of inheriting Duchenne muscular dystrophy and the daughters have a fifty percent chance of inheriting this disease to their offspring when they have kids of their own.

If a disease process such as muscular dystrophy damages a muscle fiber, some of the CK leaks out into the blood. Since there may be respiratory and cardiac problems the child would not be able to participate in high levels of activity.

An examination of a complete nervous system test includes the heart, lungs and muscles. At least half of affected boys do not walk until eighteen months of age or later. In addition, he will also work with an occupational therapist to promote more specific exercises. Dystrophin-glycoprotein is a protein that prevents damage as the muscle moves.

Individuals diagnosed with Duchenne Muscular Dystrophy are muscle weaknesses beginning with the legs and pelvis, but may spread to the arms and back, difficulty with gross-motor skills, frequent falls, and fatigue.

The last goal for the student is to actively participate in his adaptive PE class most of the time by picking the ball and throwing at a target to strengthen his muscle tone and improve his self-esteem.

Another hallmark is the apparent enlargement of the calf and sometimes other muscles, which is really due to an accumulation of fat and connective tissue in the muscle.

Examples List on Duchenne Muscular Dystrophy

Duchenne muscular dystrophy is said to cause a human to have heart disease as early as ages nineteen to twenty one. This condition may cause a person to lose their ability to walk or do any physical activity by age twelve causing the person that has Duchenne muscular dystrophy to sit in a wheel chair for the rest of their life.

Frequently, however, a wheelchair will be needed by age twelve.Distal dystrophy is one of the rare forms of muscular dystrophy that affects both men and women. It causes muscle weakness in the forearm, hands, lower legs, and feet.

Generally, distal dystrophy is less severe and it progresses very slowly than others.

Duchenne Muscular Dystrophy (DMD)

- Muscular Dystrophy: Roots, Cause, and Current Research Muscular dystrophy is an inherited disease that was discovered inby Guillaume B.A. Duchenne. Muscular dystrophy is a group of heredity disorders characterized by. Duchenne muscular dystrophy is a common X-chromosome linked muscle disorder.

It was first noted by Guillaume Benjamin Duchenne, a French neurologist, in the s. Little was known about the disease till the s when the mutated gene on the X-chromosome was identified. Duchenne muscular dystrophy may cause retardation but this disease will not cause it to get worst overtime, motor skills such as hopping, jumping, skipping, jogging, and running and can even cause a person to have difficulty walking.

Duchenne muscular dystrophy only affects boys (girls are only affected on extremely rare conditions). A problem in this particular gene, the dystrophin gene, is known to result in a flaw in one single protein, dystrophin, which is very important in muscle fibers.

Duchenne Muscular Dystrophy Number This essay discusses a condition called Duchenne muscular dystrophy and delves in to various aspects of the disease such as basic definition, description, epidemiology, pathogenicty, symptoms and diagnosis, treatment and on-going research.

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