Triple X Syndrome Research Paper

Improved Essays
Show More
Triple X Syndrome (Trisomy X) What is a genetic disorder? A Genetic disorder is inherited conditions caused by a DNA abnormality. Genetic disorders are caused by problems by one or more abnormalities in genomes. Usually apparent at birth. Genetic disorders are usually rare and impact one in several thousands, if not millions each day. For example Triple X syndrome affects 1 of 1,000 of females. Triple X Syndrome also known as (trisomy x) is a genetic disorder that deals with females having an extra X chromosome in each cell. Most females with triple X syndrome are normal with sexual development and are able to have children. Triple X syndrome goes along with a higher risk of learning disabilities and delayed development of speech …show more content…
Triple X syndrome was discovered by Patricia Jacobs in 1959. A researcher who was working in a hospital in Scotland. Patricia Jacobs discovered that Females normally have 2 X chromosomes in all cells- one X chromosome from each parent. This usually pertains to women and girls to wear as they have 3 X chromosomes. This can cause a lot of different symptoms pertaining to triple X syndrome. But some of the symptoms that come with triple X syndrome may not pertain to all with this …show more content…
Triple X Syndrome causes females to be taller than average height. With especially long legs--the most typical physical feature. Females with this disorder have delayed development of speech and language skills. Also motor skills consisting of sitting up and walking. Learning disabilities such as difficulty reading also known as dyslexia, understanding or math. This affects memory, judgement and information. Causes weak muscle tone also known as hypotonia. Abnormally curved fingers. Behavior and emotional problems. Vertical fold or skin that covers inner corners of eye. Eyes are widely spaced. Premature ovarian failure or ovary abnormalities. Infertility or menstrual irregularities. Early or late puberty. Causes constipation, abdominal pain, seizures, kidney abnormalities, frequent urinary tract infections. Flat feet also abnormally shaped breastbone. This also pertains to heart

Related Documents

  • Improved Essays

    Nt1310 Unit 1 Assignment
    • 449 Words
    • 2 Pages

    Nt1310 Unit 1 Assignment

    My choice for a genetic disorder is Spinal Muscular Atrophy also known as SMA. SMA is an inherited or genetic disorder that affects spinal motor neurons. Without these properly functioning neurons, patients have increased muscle weakness. In some severe cases patients will lose the ability to breath or swallow on their own. According to the National Human Genome Research Center, 1 in 6,000 to 1 in 10,000 people are affected by SMA.…

    • 449 Words
    • 2 Pages
    Improved Essays
    Read More
  • Great Essays

    Ap Psychology 5.1
    • 1446 Words
    • 6 Pages

    Ap Psychology 5.1

    Review Questions # 5 2. Distinguish between autosomal dominant and autosomal recessive disorders and provide a couple examples of each. When dealing with genetic disorders its important to understand how they are inherited. There are two ways a child can inherited a genetic disorder from their parents. Autosomal dominant disorder is where one parent has a genetic disorder in which it has already manifested such as familial hypercholesterolaemia, marfan’s syndrome, and achondroplasia(dwarfism) and this dominant gene is inherited by their child who will also develop the disorder.…

    • 1446 Words
    • 6 Pages
    Great Essays
    Read More
  • Improved Essays

    Trisomy 21 Research Paper
    • 1600 Words
    • 7 Pages

    Trisomy 21 Research Paper

    Describe trisomy 21. Trisomy 21 is a genetic disorder commonly known as Down syndrome. It is caused by the presence of all or part of an extra 21st chromosome. IT is the most common chromosomal abnormality associated with intellectual disability. One in 730 live births results in trisomy 21.…

    • 1600 Words
    • 7 Pages
    Improved Essays
    Read More
  • Superior Essays

    Research Paper On Duchenne Muscular Dystrophy
    • 806 Words
    • 4 Pages

    Research Paper On Duchenne Muscular Dystrophy

    Duchenne muscular dystrophy (DMD) is a one type of muscular dystrophy. Muscular dystrophy is a group of genetic disorders, leading to progressive muscle degeneration. People suffering from most common muscular dystrophies ,Duchenne/Becker (DMD), Myotonic (MMD), and Limb-Girdle (LGMD), experience muscles degradation overtime, leading to overall muscle weakness and decreased mobility. Statistics show that the most prevalent forms of muscular dystrophy are rare.…

    • 806 Words
    • 4 Pages
    Superior Essays
    Read More
  • Improved Essays

    What´s Duchenne Muscular Dystrophy?
    • 462 Words
    • 2 Pages

    What´s Duchenne Muscular Dystrophy?

    Carriers are women that have an X chromosome that has a duchenne muscular dystrophy gene. Definition of Disorder The definition of duchenne muscular dystrophy (which includes what happens to the body and what part of the body does it generally affect) is an interfer with protein production that is needed to maintain and to form a healthy muscle. It is a mutation, flaw or gene.…

    • 462 Words
    • 2 Pages
    Improved Essays
    Read More
  • Improved Essays

    Cornelia De Lange Syndrome
    • 95 Words
    • 1 Pages

    Cornelia De Lange Syndrome

    Cornelia de Lange Syndrome can also include cardiovascular concerns. Congenital heart disease occurs in approximately 25% of individuals with the disorder. The most common is ventricular septal defects, followed by atrial septal defects, pulmonary stenosis, and tetralogy of Fallot (3). Kidney problems, including renal dysplasia, pelvic dilation and vesiculoureteral reflux, can also occur (4). Abnormalities of the genitalia are common; cryptorchidism (undescended testicles) is reported in approximately 73% of males and small genitalia in 57% (3).…

    • 95 Words
    • 1 Pages
    Improved Essays
    Read More
  • Superior Essays

    Non-Classical Adrenal Hyperplasia (NCAH)
    • 975 Words
    • 4 Pages

    Non-Classical Adrenal Hyperplasia (NCAH)

    “Skeletal maturation may be significantly advanced among children with NCAH” (Witchel). The person would be overly tall as a child but have a relatively short stature as an adult. Women will develop breasts and pubic hair at early ages and may fail to menstruate in their teens (US National Library of Medicine). Men will show a lowered voice, enlarged genitals, and well developed muscles (US National Library of Medicine). If not seen in childhood, different symptoms arrive with adulthood.…

    • 975 Words
    • 4 Pages
    Superior Essays
    Read More
  • Decent Essays

    Turner Syndrome Research Paper
    • 251 Words
    • 2 Pages

    Turner Syndrome Research Paper

    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
    Read More
  • Great Essays

    How Does Down Syndrome Affect Family
    • 1829 Words
    • 8 Pages

    How Does Down Syndrome Affect Family

    This occurs when a pair of the twenty first chromosome in the egg or sperm does not properly divide, resulting in the child having three copies of chromosome 21 instead of just two. The extra copy of chromosome 21 is reproduced in every cell of the unborn child’s body. This type of Down Syndrome is more common than any other type. It is the cause behind 95% of all people with Down syndrome (“Facts about Down Syndrome”).…

    • 1829 Words
    • 8 Pages
    Great Essays
    Read More
  • Improved Essays

    Ambiguous Genitalia Essay
    • 1095 Words
    • 5 Pages

    Ambiguous Genitalia Essay

    Description and Causes The infant, depending on the sex, will first have signs of the disorder during pregnancy…

    • 1095 Words
    • 5 Pages
    Improved Essays
    Read More
  • Improved Essays

    What´s Fragile X Syndrome?
    • 441 Words
    • 2 Pages

    What´s Fragile X Syndrome?

    Fragile X syndrome is a genetic condition resulting in different types of growth problems like learning disabilities, difficulty with memory, and thinking skills. Affected individuals usually have a late development of speech and language by age two. Children with fragile X may have anxiety and abnormal behavior such as fidgeting or impulsive actions. They may have ADD, which makes it harder to pay attention and focus on specific tasks. About a third of people with fragile X have traits of autism spectrum disorders that affect communication and interaction with others.…

    • 441 Words
    • 2 Pages
    Improved Essays
    Read More
  • Improved Essays

    Fragile X Research Paper
    • 709 Words
    • 3 Pages

    Fragile X Research Paper

    This concept was peculiar to me because I assumed they would have the same symptoms as another person who has fragile X. I was unaware that the symptoms would be more or less severe. This leads into the statistic about how females are less likely to inherit the typical symptoms. That is why Denise’s daughter is much different than her son since it…

    • 709 Words
    • 3 Pages
    Improved Essays
    Read More
  • Improved Essays

    Research Paper On Fragile X Syndrome
    • 333 Words
    • 2 Pages

    Research Paper On Fragile X Syndrome

    Fragile X syndrome is the most common cause of autism in the world. Fragile X is a disease that lots of people are trying to find a cure for but so far not so much. Fragile X is one of the many genetic disorders in the world that I will be talking about Fragile X syndrome is as I said before, the most common cause of autism worldwide. This syndrome can cause anxiety learning problems, and more. Fragile X happens when the FMR1 gene is expanded.…

    • 333 Words
    • 2 Pages
    Improved Essays
    Read More
  • Improved Essays

    Genetic Disorders: Fragile X Syndrome
    • 1463 Words
    • 6 Pages

    Genetic Disorders: Fragile X Syndrome

    Fragile X syndrome (FXS) is a genetic disorder that is the most common cause of inherited mental retardation. Although often compared to autism, FXS is a comprehensive disorder, characterized by numerous physical and behavioral symptoms. FXS is a caused by trinucleotide repeats on the X chromosome, which prevents the production of the protein FMRP, that is necessary for normal brain functioning. It is important for parents, educators, and the general population to better understand this syndrome, as interventions must be targeted for the characteristics specific to FXS, rather than simply lumping it together with autism and expecting that those methods will be beneficial to the child. Fragile X syndrome affects about one out of every five…

    • 1463 Words
    • 6 Pages
    Improved Essays
    Read More
  • Great Essays

    Muscular Degenerative Disease
    • 1691 Words
    • 7 Pages

    Muscular Degenerative Disease

    During offspring, parents pass on two sets of chromosomes each. A mother always passes on an X- chromosome, letting the father pass on a Y- chromosome, deciding the gender of the child. The flawed gene passed on by the mother does not have to date back to ancestral connections, either because the family might have not known about the disease and never had a son that inherited it, or the child had a new genetic mutation in the mother’s eggs ("Diseases - DMD”). Therefore, the reason why young men are often diagnosed with this disease is according to their…

    • 1691 Words
    • 7 Pages
    Great Essays
    Read More

Related Topics

Ready To Get Started?
Discover
Company
Follow
©2024 Cram.com
Privacy Policy |  About Ads |  Site Map |  Advertise  | 
  • Cookie Settings