Thursday, January 2, 2020
Fragile X Disease Essay - 1587 Words
Fragile X is a disease which severely influences the everyday lives of those affected by it. It is a disease which unfortunately limits an individual in several respects. Physical symptoms include an elongated face with larger than normal ears and feet. Additionally, the individual will have a difficult time interacting with others due to shyness and trouble with processing faces, thus encountering behavioral road blocks. Most importantly, the individual may have intellectual disabilities such as difficulty with memory, all a result of having Fragile X. Fragile X is the most common single gene which leads to autism and other intellectual disabilities. Fragile X is transmitted through DNA. Within the DNA, it has been found that theâ⬠¦show more contentâ⬠¦As previously stated, those with more than 30 repeated trinucleotides of CGG are likely to develop some form of Fragile X (often referred to as premutation), with those having over 200 repeats having the full syndrome (also kn own as a full mutation). All of the repeated trinucleotides are located within the promotor region of the FMR1 gene. The reason the FMR1 gene produces so little FMRP is due to a process called methylation. Methylation is a process which inactivates a gene, and the larger number of repeats inactivates the gene. When the gene is inactivated, the cell may make little or none of the needed FMRP. (NICHD 2009). Figure 2: Normal promoter region VS. Elongated promoter region (NICHD 2009) Intriguingly enough, in certain cases, despite having 200+ CGG trinucleotide repeats within a FMR1 gene, it is still possible to be able to produce FMRP. One way this can be performed is by being born female. Males are born with an X and Y chromosome. Females however, are born with two X chromosomes. A female with Fragile X in one chromosome may not necessarily have Fragile X within the other chromosome. Within the female, certain cells may choose to activate one of the X chromosomes, and other cells may ch oose to activate the other X chromosome. Hence, even though there exists a Fragile X chromosome, not all cells within the body will use it, thus the production of FMRP is possible using the other normal X chromosome.Show MoreRelatedPrevention For Disease Control And Prevention1428 Words à |à 6 PagesAccording to the forecasted statistics of Center for Disease Control and Prevention (2014), the public health research will most likely provide a better diagnostic resolution to the health concern of FXS in 2020 (Center for Disease Control and Prevention, 2014). The agency based its claim from the steady decline of families reporting that they are having a hard time dealing with FXS. Per CDC (2014), this only means that the public is becoming more aware of this condition. Their participation contributesRead More The Neurobiology of Mental Retardation: Fragile X Syndrome Essay1549 Words à |à 7 PagesRetardation: Fragile X Syndrome In my previous paper, I wrote on the topic of the nature-nurture debate and the ways it related to the brain-equals-behavior dilemma. In this paper, I will continue this investigation into the link between genes and neurobiology, but I will focus in on a particular aspect of the relationship: neurological disease caused by genetic aberration. There are many well studied and well documented (thought not necessarily well understood) disorders associated with the X chromosomeRead MoreThe Genetic Mutation Fragile X Syndrome Essay922 Words à |à 4 PagesThe genetic mutation Fragile X syndrome is the most commonly inherited form of intellectual disability. Because the disease was first studied in 1943 by British physician James Purdon Martin and British human geneticist named Julia Bell, Fragile X is also referred to as Martin-Bell syndrome. Though it was not until 1969 that scientist Herbert Lubs discovered what exactly causes Fragile X syndrome. He explained that those who obtain th e mutation will possess an X chromosome with an unusual gapRead MoreWhat is Autism?1999 Words à |à 8 Pages 5671). Fragile X syndrome (FXS) is the most common inherited form of intellectual disability and is universally recognized as the monogenic cause of Autism. The gene responsible for Fragile X Syndrome, FMR1, is located on the long arm of the X chromosome. It contains a CGG repeat sequence in the 5ââ¬â¢-untranslated region that, on expansion to greater than 200 repeats, results in gene methylation and transcriptional silencing of the FMR1 gene. The absence of its protein product, fragile X mental retardationRead MoreCommunicating with Fragile X Syndrome Children Essay2092 Words à |à 9 Pages4,000 males and 1 in 8,000 females are affected by Fragile X Syndrome(CDC)? Fragile X Syndrome affects does not only affect the young or the old but it will affect anyone of any age. Children who have Fragile X Syndrome can learn many different ways of communicating with others. Al so there are many ways to help a Fragile X children become more socially active. There are many ways to help Fragile X Syndrome children to communicate. Fragile X Syndrome effects people of all ages from birth tillRead MoreThe Genetic Factors of Learning Disabilities Essay3049 Words à |à 13 Pageslearning disorder that I would like to discuss is Fragile X syndrome. Fragile X, often called Martin-Bell syndrome for itââ¬â¢s the man who discovered it is a trinucleotide repeat disorder that is found on the sex chromosome X. Fragile X was discovered by Bell in 1943 after he examined a family in which all the boys showed signs of mental retardation. He discovered that the boys X chromosome he found that the long arm had become thin and fragile looking. Fragile X affects the genders separately due to its locationRead MoreThe Genetic Mutation Fragile X Syndrome Essay960 Words à |à 4 PagesThe genetic mutation Fragile X syndrome occurs on a segment of human DNA. Because the disease was first studied in 1943 by British physician James Purdon Martin and British human geneticist named Julia Bell, Fragile X is also referred to as Ma rtin-Bell syndrome. Though it was not until 1969 that scientist Herbert Lubs discovered what exactly causes Fragile X syndrome. He explained that those who obtain the mutation will possess an X chromosome with an unusual gap. The gap located on the chromosomeRead MoreEssay on Fragile X Syndrome1374 Words à |à 6 Pagesmental impairment is Fragile X Syndrome. Fragile X Syndrome is a mental retardation that affects social, learning and intellectual disabilities. It is a result of a change and mutation in a single gene, which can be pasted on to future generations. Symptoms arise when the mutated gene, FMR1, cannot produce enough of the protein, FMRP, that the bodyââ¬â¢s cells need to function. The symptoms can vary from each affected individual depending on how severe the gene mutation is. Fragile X causes symptoms suchRead More The Etiology of Autism Essay1704 Words à |à 7 Pagesidentification of this disease, hypothesized that autism might be a biological disorder as op posed to a psychological one. Numerous studies have been conducted supporting Kannerââ¬â¢s hypothesis. These studies have ranged from examining the effects of rubella to investigating certain purine metabolic disorders as possible etiological agents. Recently, the areas of neuroanatomy, neurochemistry, and genetics have played a crucial role in developing a clearer picture into the etiology of this disease. Upon exploringRead MoreGenetic Disorders and Down Syndrome Essay969 Words à |à 4 Pagesdisorder is a disease that is caused by an abnormality in an individuals DNA. Abnormalities can range from a small mutation in a single gene to the addition or subtraction of an entire chromosome or set of chromosomesâ⬠(Letsou). Most individuals are either related to or know someone who is effected by some type of disability. Many of these disabilities are caused by genetic disorders. Genetic disorders may alter physical appearance and cause mild to severe mental retardation. Fragil e X syndrome, Down
Subscribe to:
Post Comments (Atom)
No comments:
Post a Comment
Note: Only a member of this blog may post a comment.