Preview

Dystonia - a Case Study Describing and Analyzing the Effects of Dystonia

Better Essays
Open Document
Open Document
1371 Words
Grammar
Grammar
Plagiarism
Plagiarism
Writing
Writing
Score
Score
Dystonia - a Case Study Describing and Analyzing the Effects of Dystonia
Dystonia, a neurological condition or movement disorder wherein the neurological ‘machinery’ controlling the relaxation of muscles that are not in use function inappropriately. Abnormal messages or signals are sent from the movement control centre of the brain to the muscles of the body; these irregular transmissions cause the muscles to contract and twist into involuntary spasms, uncomfortable positions or abnormal postures.

Dystonia can affect many or single muscle groups in the body, also meaning that the symptoms can range from quite severe to minimal depending on the extent of the disorder. Dystonia is not limited to one gender and can present itself at any age. Although there are many forms of Dystonia , the disorder can be (generally) categorized into two immediate groups, primary and secondary Dystonia. Primary Dystonia is seen as a genetically based type of Dystonia and is most commonly found in children. Although primary Dystonia can be a debilitating disease, it does not usually affect the non-movement related functions of the brain meaning that the person who has the disorder would be able to comprehend their situation but not physically express themselves or live to a normal capacity in worst case scenarios. In the primary Dystonia group also resides another branch called late-onset or adult-onset primary Dystonia that is developed over the age of 30; it is presumed to be a hereditary disorder and is less common. The other type (group) of Dystonia is called secondary Dystonia. Secondary Dystonia is usually the result of injury, pressure or trauma to the brain but it can also be an unseen result of illness or disease .

Dystonia the name originated from a man called DR. Hermann Oppenheim (1858-1919); He opened a centre for clinical neurology in 1980 and wrote information on brain tumours and syphilis of the brain. In 1911 Oppenheim invented the term ‘Dystonia muscular in deformans’; the term Dystonia is used regularly in modern times. Before



References: http://www.medtronicneuro.com.au, made by Medtronic – managing movement disorders, section: improving life – by controlling involuntary movement, document title: treatment options for Dystonia, last updated: 17th December 2007, Australian site. http://www.brainaustralia.org.au, made by the brain foundation: brain Australia – an initiative of the brain foundation, section: a-z brain disorders, document title: Dystonia, last updated: September 2008, Australian site. http://www.dystonia-foundation.org, made by the Dystonia medical research foundation, section: what is Dystonia?, last updated: 2006, Canadian site.

You May Also Find These Documents Helpful

  • Better Essays

    Nt1330 Unit 9 Study Guide

    • 1207 Words
    • 5 Pages

    * Dysarthria- motor speech disorder resulting from neurological injury of the motor component of the motor-speech system.…

    • 1207 Words
    • 5 Pages
    Better Essays
  • Good Essays

    Muscular dystrophies are a group of genetic conditions characterized by progressive muscle weakness and wasting (atrophy). The Duchenne and Becker types of muscular dystrophy are two related conditions that primarily affect skeletal muscles, which are used for movement, and heart (cardiac) muscle. These forms of muscular dystrophy occur almost exclusively in males.…

    • 1511 Words
    • 6 Pages
    Good Essays
  • Good Essays

    Duchenne MD is the most common muscle dystrophy. Due to the way the disease is acquired, it generally influences young men. It is conceivable…

    • 884 Words
    • 4 Pages
    Good Essays
  • Good Essays

    Duchenne muscular dystrophy is a muscular dystrophy but in order to understand it and how it works you will need to know about genetics and how they work and after that, I can tell you about a few treatments and therapies.…

    • 1325 Words
    • 6 Pages
    Good Essays
  • Good Essays

    Duchenne Muscular Dystrophy is a dangerous and rare disorder. It’s transferred through family generations because it’s a genetic disease. In addition, Duchenne Muscular Dystrophy is referred to by other names including DMD, Duchenne Syndrome, and Pseudohypertrophy. DMD is when the body cannot make dystrophin so it results in muscle weakness.…

    • 1141 Words
    • 5 Pages
    Good Essays
  • Satisfactory Essays

    Duchenne muscular dystrophy is a genetically inherited disease that causes progressive muscle and bones weakness. The symptoms usually appear before age 6 and may appear as early as infancy. Symptoms can be noticed very early like not sitting and standing independently at the correct age. The age for walking for boys with Duchenne muscular dystrophy is around 18 months. There is progressive muscle weakness of the legs and pelvic muscles, which is caused by a loss of muscle mass. This muscle weakness can cause difficulty climbing stairs. Most Symptoms appear in boys ages 1-6. Because of muscle damage kids Might need braces by the age of 10 and by age of 12 be in be wheelchair. The amount of people using wheelchairs because of duchenne muscular dystrophy is around, 29% of males 5 through 9 years of age, 82% of males 10 through 14 years of age and more than 90% of males 15 through 24 years of age.…

    • 315 Words
    • 2 Pages
    Satisfactory Essays
  • Good Essays

    Muscular dystrophy (MD) is a group of nine neuromuscular diseases. This means it is related both to the nervous system and to the muscles. About 250,000 people in the United States have muscular dystrophy. Muscular dystrophy (MD) is a group of nine neuromuscular diseases. This means it is related both to the nervous system and to the muscles. About 250,000 people in the United States have muscular dystrophy. There are many different types of Muscular Dystrophy but how do they affect your body? Myotonic (also called MMD or Steinert's disease). The most common form of muscular dystrophy in adults, myotonic muscular dystrophy affects both men and women, and it usually appears any time from early childhood to adulthood. In rare cases, it appears in newborns (congenital MMD). The name refers to a symptom, myotonia -- prolonged spasm or stiffening of muscles after use. This symptom is usually worse in cold temperatures. The disease causes muscle weakness and also affects the central nervous system, heart, gastrointestinal tract, eyes, and hormone-producing glands. In most cases, daily living isn't restricted for many…

    • 1466 Words
    • 6 Pages
    Good Essays
  • Better Essays

    Ecstasy

    • 1456 Words
    • 6 Pages

    Duchenne muscular dystrophy symptoms can appear as early as an infant to six years old. This disease is causes many miserable symptoms that can affect a person’s ability to do many activities such as: getting up from a laying position and climbing chairs or any physical activities that has to do with using a lot of muscles. 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 can also affect your ability to learn like a normal human and may cause IQ to be as low as seventy five percent or even lower. This disease can be very dangerous as it is known to cause a person to have frequent down falls. Duchenne muscular dystrophy begins in the…

    • 1456 Words
    • 6 Pages
    Better Essays
  • Satisfactory Essays

    Muscular Dystrophy Essay

    • 446 Words
    • 2 Pages

    Muscular dystrophy (MD) is a group of genetic diseases involving progressive weakness and degeneration of the muscles that control movement. In some forms of MD, the heart muscles and other involuntary muscles, as well as other organs, are affected. There are 9 distinct types of MD.…

    • 446 Words
    • 2 Pages
    Satisfactory Essays
  • Powerful Essays

    Dem 201

    • 1182 Words
    • 5 Pages

    Derives from the Latin demens, meaning ‘without mind’, is classes as a syndrome because is a group of related symptoms that are associated with a progressive decline of the brain.…

    • 1182 Words
    • 5 Pages
    Powerful Essays
  • Better Essays

    Nerve cells use a brain chemical called dopamine to help control muscle movement. Parkinson 's disease occurs when the nerve cells in the brain that make dopamine are slowly destroyed. Without dopamine, the nerve cells in that part of the brain cannot properly send messages. This leads to the loss of…

    • 1207 Words
    • 5 Pages
    Better Essays
  • Powerful Essays

    Informative Outline

    • 1631 Words
    • 5 Pages

    I. When individually researching about Parkinson’s, whether for academic reasons or personal medical reasons, the best place to start is with the diagnosis.…

    • 1631 Words
    • 5 Pages
    Powerful Essays
  • Powerful Essays

    Dystonia Case Study

    • 1653 Words
    • 7 Pages

    Dystonia is a neurological syndrome of typically patterned, often repetitive twitching movements or abnormal postures, associated with sustained or intermittent muscle contractions (23649720). These symptoms usually worsen by voluntary action of the muscle. (24978640). It can be classified in multiple ways based on, the age of onset (early or late); the topographical involvement of regions (focal - single region, segmental - two or more adjacent regions, multifocal - two or more non-adjacent regions, generalised - leg/legs and trunk with one other region, hemidystonia - ipsilateral arm and leg); the loci of gene involved; primary or secondary (drugs and neurological disorders) (14509661). Still being primitive in understanding the physiology of dystonia, synchronized contraction of agonistic and antagonistic muscle groups due to cortical over excitability and loss of inhibition at a required level of the nervous system is considered to be the possible pathophysiology of dystonia. (8752405) Amongst the early onset dystonia’s,…

    • 1653 Words
    • 7 Pages
    Powerful Essays
  • Good Essays

    Restless Legs Syndrome

    • 729 Words
    • 3 Pages

    Restless legs syndrome is a neurological disorder that has been studied for hundreds of years. The earliest documentation of the syndrome was recorded nearly 400 years ago by Thomas Willis, a 17th century English physician who served King Charles II. Willis described cases of people having trouble sleeping because of constant contractions of tendons in the legs. Soreness resulted from these contractions and would hinder sleep for days at a time. The condition he was describing was almost positively Restless Legs Syndrome (RLS), but little was known about it at the time. There were other accounts of the disease throughout the centuries and in 1923 Hermann Oppenheim discovered it to be a neurological disorder. But it wasn’t until 1944 that Professor Karl-Axel Ekbom gave the disease its current name and studied it in greater detail. RLS is also commonly known in the medical world as “Ekbom disease” because of his efforts and studies (www.restlesslegs.org).…

    • 729 Words
    • 3 Pages
    Good Essays
  • Best Essays

    Aged Care

    • 5001 Words
    • 21 Pages

    Lawlor, B. (2002). Managing behavioural and psychological symptoms in dmentia. British Journal of Psychiatry , 181:463-465.…

    • 5001 Words
    • 21 Pages
    Best Essays

Related Topics