Preview

Diagnosing Williams Syndrome

Satisfactory Essays
Open Document
Open Document
193 Words
Grammar
Grammar
Plagiarism
Plagiarism
Writing
Writing
Score
Score
Diagnosing Williams Syndrome
Chromosome 7 represents between 5% and 5.5% of total DNA cells and when missing you could get Williams syndrome. Williams syndrome is a genetic condition that is present at birth and can effect anyone .symptoms of Williams syndrome are learning problems, unique personality characteristics, heart blood vessel problems, dental problems. Williams syndrome can’t kill you but it will be hard to live with it.

Doctors will have you take tests to diagnose Williams syndrome .Ways doctors diagnose Williams syndrome are blood tests and the microarray test microarray takes longer but gives more information. Although we don’t have anything that can cure Williams syndrome we can make it a bit better by taking physical therapy, speech therapy, and avoiding extra calcium and vitamins due to high blood pressure.
…show more content…
Williams syndrome was estimated 1 per every 7,500 up to 10,000 people. According to my research Williams syndrome is a negative because people won’t have as well of an education as people who don’t have Williams syndrome due to chromosome 7 and family

You May Also Find These Documents Helpful

  • Good Essays

    Down syndrome- A condition that occurs when a person has three 21-chromosomes. Many people with down syndrome have problems with their heart, get lung infections easier, and are likely to eventually get leukemia and Alzheimer's.…

    • 1309 Words
    • 6 Pages
    Good Essays
  • Satisfactory Essays

    Victor Daniel Williams was accused of robbing a Victoria pizza parlour in October of 1993. The accused pleaded not guilty of this crime. Williams was of Aboriginal decent, the issue of prejudice became a factor in the case. Due to this, there was inquiry on whether or not he would be able to question the jury, challenge for cause, to make sure that they were impartial about his heritage. In his first trial, Hutchinson J. ruled in favour of the challenge for cause. This allowed two questions to be asked to the jury. For “procedural errors”, the Crown applied for a mistrial. This angered Williams saying the purpose of the mistrial was to underside the challenge for cause. Regardless, the mistrial was granted. When the second trial was put in…

    • 232 Words
    • 1 Page
    Satisfactory Essays
  • Good Essays

    Unit 14 E4 Cache

    • 433 Words
    • 2 Pages

    | * Hearing problems this is because bones of the middle and inner ear may develop differently in children with the syndrome. * Eye problems, the child may have a squint, their eyes may turn towards the nose/middle and they may need glasses as are usually short sighted or long sighted. * Bone, muscle, nerve, or joint problems * Immune system problems * Developmental delay…

    • 433 Words
    • 2 Pages
    Good Essays
  • Satisfactory Essays

    Wilms Tumor has also been linked to birth defects called syndromes. Syndromes are a group of systems linked to certain changes within the genes that could be missing or only have a half and be the cause of Wilms Tumor.…

    • 319 Words
    • 2 Pages
    Satisfactory 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.…

    • 251 Words
    • 2 Pages
    Satisfactory Essays
  • Better Essays

    Hypophosphatasia

    • 872 Words
    • 4 Pages

    Formal diagnosis criteria have not yet been established, however all forms of Hypophosphatasia share in common a reduced activity unfractionated serum alkaline phosphatase. A presence of on or two pathologic mutations in ALPL is also common. Laboratory testing is also performed and all laboratory evaluations include testing of calcium, phosphorus, magnesium, alkaline phosphate, creatinine, parathyroid hormone, and Vitamin D levels. (Hypophosphatasia, Etienne Mornet) Diagnosis is also largely sustained by measuring ALP levels in the blood. ALP level in Hypophosphatasia patients is low. It is important that doctors keep the age of the patient in mind when measuring these levels.…

    • 872 Words
    • 4 Pages
    Better Essays
  • Satisfactory Essays

    Reye syndrome is a disease that can cause irritability, confusion, loss of consciousness, and brain damage. It is a disease that can most often affect children ages 6 to 12 years old. If not addresses reye's syndrome can lead to swelling in the brain and liver damage. By looking at the cause for this disease experts were able to provide a intervention. In this paper we will examine how public health research help to serve as an intervention for reyes syndrome.…

    • 268 Words
    • 2 Pages
    Satisfactory Essays
  • Good Essays

    Gerstmann’s syndrome, though there is currently no cure, can be treated both through speech and occupational therapies. Those that suffer with Gerstmann’s syndrome can rely on aids to help overcome their deficits, such as using word processors or…

    • 592 Words
    • 3 Pages
    Good Essays
  • Better Essays

    Noonan Syndrome

    • 1686 Words
    • 7 Pages

    Noonan syndrome is a genetic disorder that was once known as Turner-like syndrome. It is a mutation of several genes where they develop proteins that are continuously active; which ends up disrupting the control of the cells growth and division resulting in abnormal developments of the body. Noonan syndrome can affect a person's physical appearance in multiple ways, along with their mental state of mind. This syndrome equally affects males and females.…

    • 1686 Words
    • 7 Pages
    Better Essays
  • Good Essays

    DiGeorge syndrome is an anomaly that occurs when the 22q11.2 chromosome has been deleted, causing many different symptoms in various parts of the body. Those affected by DiGeorge syndrome often display signs of heart disease and defect at birth, presence of "cleft" palate (opening in the roof of the mouth), learning disorders, autoimmune diseases (such as rheumatoid arthritis), hypocalcaemia (low presence of calcium in blood), speech disabilities, and sometimes growth disorders. This syndrome is not explicitly fatal, but cardiac disorders caused by the DiGeorge syndrome are its greatest cause of mortality. Diseases contracted from severe immunity deficiency can also lead to death. It has…

    • 354 Words
    • 2 Pages
    Good Essays
  • Good Essays

    Down’s syndrome is a disorder caused by a fault of the chromosomes; the pieces of DNA containing the outline for the human body. Normally a person has two copies of each chromosome but a person with Down syndrome has three copies. The extra DNA produces the physical and mental sort of Down syndrome, which include a small head that is flattened in the back, slanted eye, extra skin folds at the corners of the eyes, small ears, nose and mouth, short height, small hands and feet and some degree of mental disability.…

    • 1249 Words
    • 5 Pages
    Good Essays
  • Good Essays

    Robin Williams Disease

    • 952 Words
    • 4 Pages

    On August 11, 2014, American actor and comedian, Robin Williams took his own life, he was 63 years old. The world was devastated, saddened and confused by this tragedy. The question on everybody's mind was, why would this extremely gifted comedian and actor who won an Oscar and an extraordinary comedian take his own life when he had so much to live for? What we learned in the weeks following his death was shocking. Robin Williams had been suffering from severe depression for decades. Severe depression, a disorder that if not diagnosed early can be crippling and have tragic results. Another factor that contributed to Williams taking his own life was he had been recently diagnosed with Parkinson's disease. However, it was learned that it…

    • 952 Words
    • 4 Pages
    Good Essays
  • Good Essays

    Alzheimer's Senior Moment

    • 549 Words
    • 3 Pages

    What tests should be done to determine the cause of my symptoms? No one test can determine the presence of Alzheimer's at this time, although imaging technology now allows doctors to see plaques and tangles at an earlier stage. Doctors typically conduct a variety of tests, including a mood evaluation and complete medical history, to determine the cause of the memory issues. Your doctor should explain what tests he or she feels are needed and why.…

    • 549 Words
    • 3 Pages
    Good Essays
  • Good Essays

    The outcome of this disease is easily seen. Williams syndrome is the deletions of genes on the seventh chromosome, which alter brain functionality, cardiovascular health, energy, and physical features (Adams, 2012).…

    • 854 Words
    • 4 Pages
    Good Essays
  • Good Essays

    Alzheimer's Disease

    • 1329 Words
    • 6 Pages

    Tests of blood and urine may be done to help the doctor find any problems. There are also tests of mental abilities (tests of memory, problem solving, counting, and language). A brain CT scan may assist the doctor in ruling out a curable disorder. A scan also may show signs of normal age related changes in the brain. It may be necessary to have another scan at a later date to see if there have been further changes in the…

    • 1329 Words
    • 6 Pages
    Good Essays