"Describe a range of cause of dementia syndrome" Essays and Research Papers

Sort By:
Satisfactory Essays
Good Essays
Better Essays
Powerful Essays
Best Essays
Page 46 of 50 - About 500 Essays
  • Good Essays

    Middle Range Theory in Nursing Cindy Spain American Sentinel University Middle Range Theory in Nursing The credibility of a profession is based upon its ability to create and apply theory. Nursing as a whole has not been at the forefront of theoretical research being much more practical or hands-on in nature. Unless nurses increase the value placed on research and the body of knowledge that establishes the legitimacy of their practice then nursing will remain in a subordinate position in the

    Premium Nursing Nursing theory

    • 1011 Words
    • 5 Pages
    Good Essays
  • Good Essays

    Restless Legs Syndrome

    • 729 Words
    • 3 Pages

    Restless Legs Syndrome I. History of Disorder 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

    Premium Restless legs syndrome Sleep Dopamine

    • 729 Words
    • 3 Pages
    Good Essays
  • Better Essays

    Research explain the following different manifestations of dementia: Huntington’s disease: Huntington’s disease is a progressive brain disorder caused by a single defective gene on chromosome 4 — one of the 23 human chromosomes that carry a person’s entire genetic code.  This defect is "dominant‚" meaning that anyone who inherits it from a parent with Huntington’s will eventually develop the disease. The disorder is named for George Huntington‚ the physician who first described it in the late

    Premium Alzheimer's disease

    • 3394 Words
    • 12 Pages
    Better Essays
  • Better Essays

    Ehlers-Danlos Syndrome

    • 819 Words
    • 4 Pages

    Ehlers-Danlos Hypermobility Type: Pathophysiology and Treatment Abstract Ehlers-Danlos syndrome is a degenerative condition caused by the malformation of collagen within the body. Many different types of Ehlers-Danlos syndrome have been linked to different types of collagen malformation in different tissues. Hypermobility type Ehlers-Danlos syndrome (HT-EDS) is the most common type of Ehlers-Danlos syndrome. HT-EDS is mainly characterized by marked joint instability and mild cutaneous involvement

    Premium Collagen Connective tissue Pain

    • 819 Words
    • 4 Pages
    Better Essays
  • Good Essays

    The Post Ottoman Syndrome

    • 1233 Words
    • 5 Pages

    The Post-Ottoman Syndrome: A Never-Ending Problem In the novel War and Peace In the Middle East‚ author Avi Shlaim argues that Arab nations have been unable to escape the post-Ottoman syndrome. In particular he describes how the various powers inside and outside the region have failed to produce peace. While some of Shlaim’s arguments hinder the message‚ I agree with his overall thesis that the Middle East problems were caused and prolonged by the failure of both powers and superpowers to

    Premium Israel Middle East Gulf War

    • 1233 Words
    • 5 Pages
    Good Essays
  • Good Essays

    Guillain-Barre Syndrome

    • 379 Words
    • 2 Pages

    Research paper: Guillain-Barre’ syndrome Guillain-Barre’ syndrome is a disorder in which your body’s immune system attacks your nerves. The exact cause of this syndrome is unknown‚ but it is however often preceded by an infectious illness such as a respiratory infection or the stomach flu. Luckily Guillain-Barre’ syndrome is uncommon‚ only affecting 1 or 2 people per 100‚000. Guillain-Barre’ syndrome often begins with tingling and weakness starting in your feet

    Premium Immune system Symptoms Pneumonia

    • 379 Words
    • 2 Pages
    Good Essays
  • Good Essays

    Triple X Syndrome

    • 492 Words
    • 2 Pages

    Triple X Syndrome‚ also known as XXX Syndrome‚ is a genetic disorder affecting the sex chromosomes. Females generally posses two X chromosomes‚ one from each parents‚ but females affected by Triple X syndrome possess three X chromosomes. On average‚ Triple X Syndrome affects 1 in 1000 females. Triple X syndrome generally doesn’t occur due to inheritance‚ but is rather caused by an error in the formation of the gametes known as nondisjunction‚ resulting in the extra X chromosome. Another cause of Triple

    Premium X chromosome

    • 492 Words
    • 2 Pages
    Good Essays
  • Satisfactory Essays

    Shwachman Diamond Syndrome (SDS) is an inherited condition that affects mainly the bone marrow‚ pancreas‚ and skeletal system of the human body. Bone marrow produces new blood cells; however‚ in a patient with SDS‚ the bone marrow does not make all of the types of white blood cells making the body more vulnerable to infection. The pancreas produces enzymes that help break down and use nutrients from food. SDS results in the pancreas not producing enough of these enzymes‚ which makes it hard to digest

    Premium DNA Gene Genetics

    • 370 Words
    • 2 Pages
    Satisfactory Essays
  • Good Essays

    Broken Heart Syndrome

    • 637 Words
    • 3 Pages

    Increased Mortality among Widowers by Parkes‚ Benjamin‚ and Fitzgerald was published in the British Medical Journal in 1969. The authors goal was to determine if there was any validity to the “broken heart syndrome” and to discover what the actual mortality rate in connection with the “broken heart syndrome”. The population of this study included widowers 55 years of age and older and the sample used was 4‚486 widowers 55 years of age and older. The study was completely observation as the men were followed

    Premium Health care Medicine Patient

    • 637 Words
    • 3 Pages
    Good Essays
  • Satisfactory Essays

    Treacher Collins Syndrome

    • 251 Words
    • 2 Pages

    Treacher Collins Syndrome is believed to be caused by a change in the gene on chromosome 5‚ which affects facial development. About 40 percent of the time‚ one parent has the Treacher Collins Syndrome gene. Geneticists can now determine whether the Treacher Collins gene is a new mutation or one that has been passed on. There are new studies being done to see about the possibilities of there being other genes that could be involved with this syndrome. Treacher Collins Syndrome is believed to be

    Premium DNA Gene Genetics

    • 251 Words
    • 2 Pages
    Satisfactory Essays
Page 1 42 43 44 45 46 47 48 49 50