Free duchenne muscular dystrophy Essays and Papers.

Duchenne Muscular Dystrophy Essay Sample. Duchenne muscular dystrophy is an inherited disease that is also known as muscle weakness that gets worst after a short period of time. Duchenne muscular dystrophy is caused by defected gene for dystrophy which is a protein in the muscle that is often said to be passed down from generation from family.

WebMD explains the causes, symptoms, and treatment of Duchenne muscular dystrophy, a rare muscle disease that mainly affects mainly boys in early childhood.

The genetic disorder I have chosen to write about is Duchenne muscular dystrophy, which is a condition that cause a reduced lifespan through the progressive weakening of the muscles. In this essay I aim to describe how this disease is inherited, how it affects individuals and the current and potential treatments for Duchenne muscular dystrophy.

Duchenne muscular dystrophy is one of the nine types of muscular dystrophy and is more prominent in males than females. Duchenne MD is one of the most rapidly worsening types of muscular dystrophy and is caused by a defect in a particular muscle protein. Symptoms appear before the age of six and can be detected during infancy (A. D. A. M, 2012).

Duchenne muscular dystrophy (DMD) is a severe type of muscular dystrophy. The symptom of muscle weakness usually begins around the age of four in boys and worsens quickly. Typically muscle loss occurs first in the thighs and pelvis followed by those of the arms. This can result in trouble standing up.

Duchenne’s muscular dystrophy is a recessive genetic disorder caused by a deficiency of the protein dystrophin, which is found in muscle cells. This disorder is usually only found in males. It has very rarely been found in females because they have two X chromosomes and the disease is recessive.

Science Report Genetic Disorders- Duchenne Muscular Dystrophy (DMD) Description of disorder, symptoms and chance of survival Duchenne muscular dystrophy is a genetic disorder that causes 1 out of 3500 males' voluntary muscles that control their body's movement to progressively weaken and waste due to a lack of dystrophin.

Muscular dystrophy is defined as a group of genetic diseases in which muscle fibers are unusually susceptible to damage. These damaged muscle become progressively weaker making mobility progressively more difficult and a wheelchair becomes more of a necessity. The most common form of muscular dystrophy is Duchenne muscular dystrophy (DMD).

In boys with Duchenne muscular dystrophy, muscle weakness tends to appear in early childhood and worsen rapidly. Affected children may have delayed motor skills, such as sitting, standing, and walking. They are usually wheelchair-dependent by adolescence. The signs and symptoms of Becker muscular dystrophy are usually milder and more varied.

The diagnostic process often involves a series of steps to confirm Duchenne. Getting a formal diagnosis and understanding your child's specific mutation is a critical step in determining a path for care, whether that is managing the disease or participating in clinical trials for possible treatments.. Parent Project Muscular Dystrophy (PPMD).

Duchenne (doo-SHEN) muscular dystrophy (DMD) is a rare genetic condition that weakens your child’s muscles. It is the most common muscular dystrophy, a kind of inherited muscle disease. DMD causes weakness and muscle loss that spreads throughout your child’s body.