Turner Syndrome Diary

Great Essays
Natalie Recker
Mrs. Smith
Biology- period 4
11 March 2017
Journal Entry- Day in the Life It is 9:30 P.M., and today has been a rough day. The first thought I had this morning was, ‘Will I have a good day or a bad day?’ Right after thinking that, I thought, ‘How will my Turner Syndrome diagnosis affect today?’ This, however, isn’t the first time thinking these thoughts. In fact, I ask myself these questions every day when I wake up. Every day, I struggle knowing I have a genetic disorder; Turner Syndrome. Turner Syndrome, or TS, is a genetic, chromosomal disorder in which a female is born with only one X chromosome (the 23rd pair). This affects the development in women (the disease can only occur in women). The most common way a female can get TS is by monosomy, which means an X chromosome is completely
…show more content…
When I was a kid, I would have to give myself a growth hormone shot every night. I no longer give myself these shots. The life expectancy for a woman with TS, like myself, is 50 years. The life reduction is up to 13 years. One of my favorite organizations I have been a part of is the Turner Syndrome Foundation. It has helped me very much throughout my entire life. Their tag line is, “
Turner Syndrome affects 1 in 2,000 females. We can help.” I love this foundation and everything it has helped me with. Another amazing organization is Turner’s Syndrome Society of the United States. Other interesting information I found today at work was: the average height of a woman with TS who is untreated is 4” 8’. Turner’s Syndrome is not preventable or curable, but there are treatments like the ones I stated above. Another interesting fact is that most women with TS aren’t able to have children because they are missing one of the X chromosomes. Finally, women who have TS are at higher risk of getting sick (more often) and developing another

Related Documents

  • Improved Essays

    ichael explains his case in a creative way. He has Down syndrome when the chromosomes came to make him, a normal chromosome broke, the broken piece moved and struck onto another chromosome. Its called spontaneous translocation. No one knows why this happens or how to prevent it. He starts to talk like how he is like everyone else.…

    • 642 Words
    • 3 Pages
    Improved Essays
  • Decent Essays

    Mar Fans Syndrome affects roughly 1 in 5000 people. It affects men and women in all races and roughly 3 out of 4 people inherit the syndrome from their parents. The mar fan syndrome affects many parts of the body, which means it varies from person to person. Some signs of the syndrome are: a tall thin build, long arms, fingers, toes.…

    • 213 Words
    • 1 Pages
    Decent Essays
  • Improved Essays

    Five to 10 girls with triple x syndrome are born in the united states each day. Some of the symptoms are they are taller than average height with especially long legs, delayed development of speech and language skills as well as motor skills such as sitting up and walking, and they have some learning disabilities, such as difficulty with reading, understanding or math. Triple x syndrome is genetic and usually not inherited, it's due to an error in cell division. The error can happen before conception or early in embryo's development, resulting in one of these forms of triple x syndrome.…

    • 459 Words
    • 2 Pages
    Improved Essays
  • Improved Essays

    Wolf Hirschhorn Syndrome (WHS) Wolf Hirschhorn Syndrome (WHS) is a genetic disorder caused by a deletion (the removal or obliteration of written or printed matter) in the genetic material near the short (p) arm of chromosome 4 (also written as 4p). The Genetic Home Reference tells us that “ there are two copies of chromosome 4, one copy inherited from each parent” (Genet). However big or small the individual with WHS is, then the size of the deletion changes. The bigger the deletion the more severe the symptoms become. Men are the gene holders for WHS although it is not usually inherited (Battaglia).…

    • 551 Words
    • 3 Pages
    Improved Essays
  • Improved Essays

    All cell organisms have this chain of nucleotides that give them a unique coding that helps everything differ from one another. Whether within plant or animal cells, these coding strands contain our genetic information. The creation of our genetic codes derives from a mixture of our parent genetic codes. These codes we contain are called DNA, also known as deoxyribonucleic acid. These DNA strands carry all our information.…

    • 652 Words
    • 3 Pages
    Improved Essays
  • Decent Essays

    Tuberous Sclerosis, or TSC, is a genetically inherited disease that is characterized by the numerous benign tumors in many parts of the body. It can cause symptoms such as developmental delay, autism, tumor, and skin abnormalities. Tuberous Sclerosis is caused by a mutation on the TSC1 gene located on chromosome 9 or the TSC2 gene located on chromosome 16. These genes make a protein called tuberin, and scientist believe Tuberous Sclerosis is caused when those genes mutate and produce more tuberin which would then allow the tumors to grow. However, only one of the genes needs to be affected for Tuberous Sclerosis to show up, so this makes this gene very rare.…

    • 468 Words
    • 2 Pages
    Decent Essays
  • Decent Essays

    What if you were already ten years old and just now were diagnosed with a syndrome that could have been found close to 10 years ago. Turner syndrome affects "1 in 2,500 every newborn girl," in the U.S. Turner syndrome is when a female has one working X-chromosome and one is altered or missing. The many symptoms include short stature, webbed neck and lymphedema, which is swelling of the hands and feet. To find out if you or a female you know has turner syndrome testing includes a lab test of your blood. Some people with turner syndrome can be diagnosed before they are even born but most are not diagnosed until as late as ages 5 to 10.…

    • 251 Words
    • 2 Pages
    Decent Essays
  • Great Essays

    Sickle Cell Trait Essay

    • 1570 Words
    • 7 Pages

    More research is needed to find out why some people with SCT have…

    • 1570 Words
    • 7 Pages
    Great Essays
  • Superior Essays

    Rett Syndrome Report

    • 1172 Words
    • 5 Pages

    Rett Syndrome Report Cathy Qian Clinical features Rett Syndrome (RTT) is a genetic disease which presents with a seemingly normal development up until 1-3 years of age. The disease is only present in females, as it is an X-linked dominant disorder and males with a defective X chromosome die prematurely. It is rare, with an estimate of 1:10000 - 1:15000 live female births. (4)…

    • 1172 Words
    • 5 Pages
    Superior Essays
  • Improved Essays

    Duchenne Muscular Dystrophy In this world, there are many diseases that are being caused by the X chromosomes or the Y chromosomes. Some of the diseases could be passed down from generation onto the next because it is gene and some of the diseases can be treated and which later on causes for it to make it worse. The diseases that would always be there would be Down Syndrome, Huntington’s Disease, Hemophobia, and many more.…

    • 824 Words
    • 4 Pages
    Improved Essays
  • Improved Essays

    Kennedy's Disease

    • 411 Words
    • 2 Pages

    Introduction How do you define Kennedy’s disease? Kennedy’s disease is a rare inherited disease that disturbs the males in the family by progressively weakening and wasting the motor neurons in the muscles (Kennedy's Disease Association, 2015). Kennedy’s disease got its name from the studies by Dr. William R. Kennedy who found patients with the rare disorder back in 1968, which had occurred in the later part of the adult life. Kennedy’s disease starts to appear in males between the ages of 30 to 50 years old.…

    • 411 Words
    • 2 Pages
    Improved Essays
  • Improved Essays

    Only a person who is born with the abnormal mutated gene can get the illness and pass it on to their children. People at-risk of the disease have a choice of being tested or not, some believe there is no point because it may happen eventually and there is no cure while others want to make decisions on their way of life based on the test results. Also although the testing on children is typically prohibited before the age of 18, they can be tested for early onset also known as juvenile onset HD. Testing is also an option for pregnant women Pre-genetic diagnostic (PGD) with In Vitro Fertilization (IVF) which will check whether or not the fetus will have the mutated gene. There is no cure for the disease but symptoms associated with the disease can be helped with certain medications to control emotional and movement…

    • 749 Words
    • 3 Pages
    Improved Essays
  • Improved Essays

    Apert Syndrome Essay

    • 794 Words
    • 4 Pages

    “The recurrence risk for an unaffected parent of a child with Apert Syndrome is minor, but an affected person has a 50% risk of having a baby with the syndrome” (NIH 2016).Studies have shown that pregnancies with men over the age of forty have a higher risk of developing this disorder. There is no sexual predilectation ,but is more prevalent in Asians. This gene produces a protein called fibroblast growth factor receptor 2. Among its multiple functions, this protein signals immature cells to become bone cells during embryonic development. According to Saritha et al.…

    • 794 Words
    • 4 Pages
    Improved Essays
  • Improved Essays

    Fragile X Syndrome Essay

    • 488 Words
    • 2 Pages

    Fragile X Syndrome Fragile X syndrome or simply Fragile X is the most common inherited form of intellectual disability. Cause(s) of the disorder Fragile X syndrome occurs because the mutated gene (FMR1) cannot produce enough of a protein known as Fragile X Mental Retardation Protein or FMRP that is needed by the body's cells, particularly cells in the brain, to develop and function normally. Those with Fragile X will either have the CGG code repeat about 55 to 200, which is known as a permutation, or more than about 200 repeats known as a full mutation. Who does it affect?…

    • 488 Words
    • 2 Pages
    Improved Essays
  • Improved Essays

    Gender Theory Paper For centuries it seems that society has always had a say on gender roles. Men and women think of the characteristics of being male or female and assume that those characteristics make up what gender is. Thinking about gender as what makes a man or a woman, people enforce these perspectives on children by praising or rejecting behaviors that may not fit the category of male or female.…

    • 1065 Words
    • 4 Pages
    Improved Essays