This essay critically examines the nature of duchenne muscular dystrophy. The condition, affecting 1 out of 3,600 boys, is an inheritable disorder arising due to mutation of the dystrophin gene. To a great extent, duchenne muscular dystrophy can be effectively managed by controlling the symptoms that lead to its development.
History: The first historical account of muscular dystrophy appeared in 1830, when Sir Charles Bell wrote an essay about an illness that caused progressive weakness in boys. In the 1850s, descriptions of boys who grew progressively weaker, lost the ability to walk, and died at an early age became more prominent in medical journals.
Duchenne muscular dystrophy: the basics Duchenne muscular dystrophy, sometimes shortened to DMD or just Duchenne, is a rare genetic disease. It primarily affects males, but, in rare cases, can also affect females. Duchenne causes the muscles in the body to become weak and damaged over time, and is eventually fatal.
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’s Muscular Dystrophy Duchenne’s muscular dystrophy (DMD) is a progressive genetic disorder that leads to muscle atrophy and eventually death. Diagnosing DMD consists of blood tests, genetic testing, and muscle biopsies. Signs and symptoms begin presenting in toddlers with DMD and progressively worsen throughout life.
BACKGROUND AND PURPOSE: Duchenne muscular dystrophy (DMD) is a lethal progressive pediatric muscle disorder and genetically inherited as an X-linked disease that caused by mutations in the dystrophin gene. DMD leads to progressive muscle weakness, degeneration, and wasting; finally, follows with the premature demise.Learn More
The cause of Duchenne Muscular Dystrophy is the occurrence of mutations in the Dystrophin (DMD) gene. The cytogenetic location off the DMD gene is Xp21.2; meaning at location 21.2 on the short arm of the X chromosome from base pair 31,119,219 to base pair 33,339,609.Learn More
Duchenne muscular dystrophy (DMD) is the most common and most rapidly progressive muscular dystrophy, with most patients losing the ability to walk by 12 years of age and requiring ventilatory support by 25 years of age. Before the use of cardioprotective drugs and respiratory muscle aids, respir.Learn More
In this review, we discuss the therapies used in the treatment of patients with Duchenne muscular dystrophy since the first description of the disease. A short description is given of the various.Learn More
Duchenne muscular dystrophy is the most common childhood form of the disease; it occurs in one of every 3,300 male births. It is a sex-linked disorder, meaning that it strikes males almost exclusively. The disease is caused by a defective gene on the 23rd, or X, chromosome that results in the failure of the body to produce a functional muscle protein called dystrophin.Learn More
Such as, Duchenne muscular dystrophy, Becker dystrophy, Emery- Dreifuss Muscular dystrophy, Myotonic muscular dystrophy, Limb- Gridle dystrophy, Facioscapulohumeral muscular dystrophy, Congenital dystrophy, Oculopharyngeal muscular dystrophy and Distal muscular dystrophy. Duchenne Dystrophy occurs 2 out of every 10,000 young men. It is the most severe disease out of all of the muscular.Learn More
Duchenne Muscular Dystrophy Essay Sample. In this assignment the author will explore Duchenne Muscular Dystrophy and the role of the community nurse. The author will explore the assessment, challenges and role of the community nurse in order to gain a better understanding of Community Health Nursing. The following is the case study to which the.Learn More
Duchenne muscular dystrophy (DMD) is a common disorder affecting the muscular system. This form of muscular dystrophy is inherited and is caused by a genetic mutation that affects the dystrophin proteins of the muscles. Dystrophin is the largest gene known to man. (Tennyson, Klamut, Warton 1995).Learn More
Duchenne muscular dystrophy (DMD) is the second most common single gene disorder in Western countries and has been recognized as a distinct entity for over 100 years.Learn More
The muscular dystrophies are an inherited group of progressive myopathic disorders resulting from defects in a number of genes required for normal muscle function. Muscle weakness is the primary symptom. The clinical characteristics and diagnosis of the Duchenne and Becker muscular dystrophies are reviewed here.Learn More
Duchenne muscle dystrophy is a progressive inherited myopathy with an early onset in childhood. 1 It progresses to the bed-bound state in the second decade of life and patients usually succumb to respiratory or cardiac complications.Learn More
Duchenne muscular dystrophy, also known as DMD, is a severe inheritable genetic condition without a cure, which becomes evident in young males, aged 1 to 6. This disorder results from a frame-shifting mutation in the DMD gene, the third largest gene in the body, which is responsible for a muscle protein named Dystrophin.Learn More