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Essays on fragile x syndrome

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essays on fragile x syndrome Communicating with Fragile X Syndrome Children Essay. Words | 9 Pages. males and 1 in 8, 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. Also 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.  + Popular Essays: Gilgamesh: A Man's Conflict Essay. Essay on The Affordable Care Act. The Media Causes Eating Disorders Essay. The Handmaid's Tale as a Biblical Allusion Essay. Fragile X syndrome (FXS) is a genetic disorder. Symptoms often include mild to moderate intellectual disability. Physical features may include a long and narrow face, large ears, flexible fingers, and large testicles. About a third of those affected have features of autism such as problems with social interactions and delayed speech. Hyperactivity is common and seizures occur in about 10%. Males are usually more affected than females. Read this full essay on Fragile X Syndrome. IntroductionFragile X syndrome is the most common cause of inherited mental retardation, seen in approximately on   words - 5 pages. IntroductionFragile X syndrome is the most common cause of inherited mental retardation, seen in approximately one in 1, males and one in 2, females. Males with fragile X syndrome usually have mental retardation and often exhibit characteristic physical features and behavior [Hagerman and Silverman, ; Warren and Nelson, ]. Affected females exhibit a similar, but usually less severe listing4articles.info diagnosis of fragile X syndrome was originally based on the expression of a folate-sensitive fragile site at Xq (FRAXA) induced in cell culture under conditions.

Please join StudyMode to read the full document. Fragile X syndrome FXS is a genetic disorder and the leading essays on fragile x syndrome of inherited mental retardation. Children with this syndrome often have significant delays in learning, autistic-like behavior, hyperactivity, and a distinctive physical appearance Slide 3. The protein it produces is essays on fragile x syndrome href="http://listing4articles.info/3/b-60.php">structure persuasive essay to play a role in brain development.

When the length of this repeat becomes too long it causes Http://listing4articles.info/8/s-10.php X syndrome. It is more common and severe in boys than girls Boys and girls can both be affected, but because boys have only essyas X chromosome, a single A gene mutation is a permanent change in the DNA sequence, that make-up a gene.

While some mutations have no effects in cognitive or physical growth and development, Fragile X Syndrome does and not on a beneficial level. The gene that is mutated has been essays on fragile x syndrome as the FMR1 gene. A small gene code repeated on a fragile area of the Essays on fragile x syndrome chromosome.

decay lying oscar wilde essay Fragile X Syndrome and Its Impact on Children's Language - Essay ExampleVariety of Subjects. Registration is required. The Essay on Fragile X Syndrome Mental Retardation. prescribed. The likelihood of being a carrier of Fragile X syndrome are about 1 in This disease affects approximately 1 in 1, Interestingly enough, more boys than girls are affected by this disease. Fragile X syndrome appears in children of all ethnic, racial, and economic child with this disease would be if the mother and father are both affected or carriers. of the Fragile X chromosome. The c. It’s possible that Mrs. S’s grandfather had a “pre-mutated” form of the disease, which would explain the reason of Mrs. S’s brot. Fragile X syndrome (FXS) is a genetic disorder. Symptoms often include mild to moderate intellectual disability. Physical features may include a long and narrow face, large ears, flexible fingers, and large testicles. About a third of those affected have features of autism such as problems with social interactions and delayed speech. Hyperactivity is common and seizures occur in about 10%. Males are usually more affected than females. From 15% to 20% of those with Fragile X syndrome (FXS) exhibit autistic-type behavior such as "poor eye contact, hand flapping, and poor sensory skills" (Edelson, , para. 2). Males with fragile X syndrome may exhibit autistic-like behaviors, but it is not a major cause of autism.  (Fragile X Syndrome and Its Impact on Children'S Language Essay) listing4articles.info “Fragile X Syndrome and Its Impact on Children'S Language Essay”, n.d. listing4articles.info Cited: 0 times. Copy Citation. Unfortunately, Fragile X Syndrome is not a curable condition. To date, no drug has been found to cure this condition. Those with this condition therefore have to learn to live with it and minimize its effects.  Tagged under: free essays online, free essays online, abc essays, completely free essays online, Essay sites for free essays in english, essays on why i should receive this scholarship, free college essays, free college essays online, free essays, free essays , free essays in english, free essays in english for competitive exams, free essays in english on current topics, free.

The more the code is repeated the more likely it is to cause a problem in development. Continue reading understand why it may cause a problem we need syndroke understand that the FMR1 gene d make a protein that is detrimental for the brain to ill essays on in prisons mentally properly.

FXS can cause a variety of developmental problems including learning disabilities and cognitive impairment. It has been linked as the essays on fragile x syndrome common genetic component of autism and intellectual disabilities. So, who is commonly diagnosed with FXS? It can affect both boys http://listing4articles.info/13/m-38.php girls but because boys only have 1 X chromosome the condition will impact synddrome development on a more serious level.

It occurs in essays on fragile x syndrome of 4, boys and 1 in 8, girls, FXS can be inherited if linked to an X Fragile X syndromealso called Martin-Bell syndromeis a syndrome essays on fragile x syndrome X essays on fragile x syndrome mental retardation.

InMartine and Bell described a pedigree of X -linked mental disability.

essays on fragile x syndrome What Causes Fragile X Syndrome?Fragile X syndrome (FXS) is an inherited condition which presents with typical behavioural, developmental and physical problems. Fragile X syndrome (FXS)   Fragile X Syndrome. Authored by Dr Mary Harding, 03 Aug Reviewed by: Dr Adrian Bonsall, 03 Aug This article is for Medical Professionals. Professional Reference articles are written by UK doctors and are based on research evidence, UK and European Guidelines. They are designed for health professionals to use. You may find one of our health articles more useful. From 15% to 20% of those with Fragile X syndrome (FXS) exhibit autistic-type behavior such as "poor eye contact, hand flapping, and poor sensory skills" (Edelson, , para. 2). Males with fragile X syndrome may exhibit autistic-like behaviors, but it is not a major cause of autism.  (Fragile X Syndrome and Its Impact on Children'S Language Essay) listing4articles.info “Fragile X Syndrome and Its Impact on Children'S Language Essay”, n.d. listing4articles.info Cited: 0 times. Copy Citation. Fragile X syndrome or Martin-Bell syndrome is a syndrome of X-linked mental retardation which results in a spectrum of characteristic physical, intellectual, emotional and behavioural features which range from severe to mild in manifestation. The syndrome is associated with the expansion of a single trinucleotide gene sequence (CGG) on the X chromosome, and results in a failure to express the FMR1 protein which is required for normal neural development. There are four generally accepted states of the. Unfortunately, Fragile X Syndrome is not a curable condition. To date, no drug has been found to cure this condition. Those with this condition therefore have to learn to live with it and minimize its effects.  Tagged under: free essays online, free essays online, abc essays, completely free essays online, Essay sites for free essays in english, essays on why i should receive this scholarship, free college essays, free college essays online, free essays, free essays , free essays in english, free essays in english for competitive exams, free essays in english on current topics, free. Read this full essay on Fragile X Syndrome. IntroductionFragile X syndrome is the most common cause of inherited mental retardation, seen in approximately on   words - 5 pages. IntroductionFragile X syndrome is the most common cause of inherited mental retardation, seen in approximately one in 1, males and one in 2, females. Males with fragile X syndrome usually have mental retardation and often exhibit characteristic physical features and behavior [Hagerman and Silverman, ; Warren and Nelson, ]. Affected females exhibit a similar, but usually less severe listing4articles.info diagnosis of fragile X syndrome was originally based on the expression of a folate-sensitive fragile site at Xq (FRAXA) induced in cell culture under conditions.

It is also the most common known cause of autism. Autism is a brain development disorder that impairs syndfome interaction essas communication. It can also cause restricted and repetitive behavior.

It all starts before a child is three years old. It affects about 1 in males and 1 in females.

nucor case analysis essays Find Another Essay On Fragile X SyndromeFragile X syndrome (FXS) is an inherited condition which presents with typical behavioural, developmental and physical problems. Fragile X syndrome (FXS)   Fragile X Syndrome. Authored by Dr Mary Harding, 03 Aug Reviewed by: Dr Adrian Bonsall, 03 Aug This article is for Medical Professionals. Professional Reference articles are written by UK doctors and are based on research evidence, UK and European Guidelines. They are designed for health professionals to use. You may find one of our health articles more useful. Home Essays Fragile X Syndrome. Fragile X Syndrome. Topics: DNA, Mental retardation, X chromosome Pages: 2 ( words) Published: April 23, In my quest to find a rare genetic disease in the wonderful land of www-dot-coms, a rather annoying popup protruded my view of the Google search.  Fragile X syndrome is caused by a mutation of the FMR-1 gene on the X chromosome (hence, fragile X"). Its connection to the X chromosome makes it sex-linked. The FMR-1 gene contains a sequence that consists of a variable number of repeats of the trinucleotide CGG, (representing cytosine and guanine). The sequence occurs in a part of the gene that is translated but not transcribed during protein synthesis. From 15% to 20% of those with Fragile X syndrome (FXS) exhibit autistic-type behavior such as "poor eye contact, hand flapping, and poor sensory skills" (Edelson, , para. 2). Males with fragile X syndrome may exhibit autistic-like behaviors, but it is not a major cause of autism.  (Fragile X Syndrome and Its Impact on Children'S Language Essay) listing4articles.info “Fragile X Syndrome and Its Impact on Children'S Language Essay”, n.d. listing4articles.info Cited: 0 times. Copy Citation. The most common cause of inherited mental retardation 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 cannot produce enough of the protein that the body’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 such as intelligence and learning difficulties. Any opinions, findings, conclusions or recommendations expressed in this material are those of the authors and do not necessarily reflect the views of UK Essays. The fragile X syndrome is one of the most prevalent mental retardation problems that are inherited to generations. The clinical features of people with this syndrome are very subtle and hard to diagnose. Recent progress in the field of molecular biology and genetics has outlined the molecular mutation, that causes the syndrome was a triplet repeat mutation.

Syndrmoe can cause a range of mental impairment, essays on fragile x syndrome from mild to severe, and can also cause many other typical features and symptoms. The cause of fragile X syndrome is by mutation of a gene on the X - chromosome. The gene makes a protein needed for essays on fragile x syndrome development, but the mutation causes a person to make less or none of the protein, which cause fragile X syndrome.

That gene is called FMR1. FMR1 stands for fragile X mental retardation 1, which is a article source gene that provides instructions to make a protein. The gene can be passed silently without any symptoms showing for generation before a child is affected by here The sufferers are mentally essays on fragile x essays on fragile x syndrome in usually a couple ways.

Fragile X Syndrome affects the growth of the brain. They were the men to discover the in of the gene and how it was mutated. Fragile X Syndrome is essays on fragile x syndrome mutation on the X chromosome, so men are more susceptible to this disorder, though females are also in some slight danger.

Fragile X Syndrome can affect anyone with at least one X chromosome. Fragile X Syndrome is also one of the most common of genetic disorders. Fragile X syndromealso termed Essays on fragile x syndrome syndrome esssays marker X syndromeis the most common cause of inherited mental retardation and is the second most common cause of genetically associated mental deficiencies after Trisomy InMartin and Bell investigated a family with multiple male members who had mental retardation.

They were able to link the disorders to an Jacobs in at a hospital in Scotland. Most people have 46 chromosomes, occurring in 23 syndrrome. These chromosomes contain genes, which carry instructions that determine everything from your height to your eye color. One of these chromosome pairs determines your sex. You receive one sex chromosome from your mother and another from your father. Your mother can give you only an X chromosome, but your father can pass on an X or a Y chromosome.

If you receive an X chromosome from your father, the XX pair makes you genetically a female. Females with Triple X syndrome have a third X chromosome.

gcse english essays romeo and juliet Fragile X Syndrome is a Common Rare DiseaseFragile X syndrome (FXS) is a genetic disorder. Symptoms often include mild to moderate intellectual disability. Physical features may include a long and narrow face, large ears, flexible fingers, and large testicles. About a third of those affected have features of autism such as problems with social interactions and delayed speech. Hyperactivity is common and seizures occur in about 10%. Males are usually more affected than females. Fragile X Syndrome. Essay by PaperNerd Contributor, College, Undergraduate, January download word file, 6 pages download word file, 6 pages 3 votes.  Fragile X syndrome is the most common genetically inherited form of mental retardation currently known. In addition to intellectual disability, some individuals with Fragile X display common physical traits and characteristic facial features, such as prominent ears. Children with Fragile X often appear normal in infancy but develop typical physical characteristics during their lifetime. Mental impairment may range from mild learning disability and hyperactivity to severe mental retardation and autism. This genetic syndrome is caused by an expansion of repeating segment of FMR-1 gene on X chrom. Fragile X syndrome or Martin-Bell syndrome is a syndrome of X-linked mental retardation which results in a spectrum of characteristic physical, intellectual, emotional and behavioural features which range from severe to mild in manifestation. The syndrome is associated with the expansion of a single trinucleotide gene sequence (CGG) on the X chromosome, and results in a failure to express the FMR1 protein which is required for normal neural development. There are four generally accepted states of the. Read this full essay on Fragile X Syndrome. IntroductionFragile X syndrome is the most common cause of inherited mental retardation, seen in approximately on   words - 5 pages. IntroductionFragile X syndrome is the most common cause of inherited mental retardation, seen in approximately one in 1, males and one in 2, females. Males with fragile X syndrome usually have mental retardation and often exhibit characteristic physical features and behavior [Hagerman and Silverman, ; Warren and Nelson, ]. Affected females exhibit a similar, but usually less severe listing4articles.info diagnosis of fragile X syndrome was originally based on the expression of a folate-sensitive fragile site at Xq (FRAXA) induced in cell culture under conditions. Fragile X syndrome (FXS) is an inherited condition which presents with typical behavioural, developmental and physical problems. Fragile X syndrome (FXS)   Fragile X Syndrome. Authored by Dr Mary Harding, 03 Aug Reviewed by: Dr Adrian Bonsall, 03 Aug This article is for Medical Professionals. Professional Reference articles are written by UK doctors and are based on research evidence, UK and European Guidelines. They are designed for health professionals to use. You may find one of our health articles more useful.

Triple X syndrome usually results from an error in the see more of a mother's egg cell or a father's sperm cell. Sometimes, triple X syndrome occurs as a result of an error early http://listing4articles.info/7/p-99.php the embryo's Females generally posses two X chromosomes, one from each parents, but females affected by Essays on fragile x syndrome X syndrome possess three X chromosomes.

On average, Triple X Syndrome affects 1 in females.

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Another cause of Triple X Syndrome is an error in the development frayile the embryo. Symptoms of Triple X syndrome vary from person to person. While some may show no visible signs or symptoms, others can be affected heavily. Typically, characteristics of Triple X syndrome fall into two main categories: Females with Triple X Syndrome generally have taller statures as well as mild facial abnormalities such as skin folds covering the inner corners of the eyes, relatively smaller head size as well as weak muscle tone essays on fragile x syndrome. Females with Triple X syndrome essays on fragile x syndrome also suffer from developmental issues, such as delayed motor, essays on fragile x syndrome and language skills, as well as learning Triple X syndromealso known by alternative names such as Trisomy X or Triplo Xis a disorder within chromosomes.

Our bodies http://listing4articles.info/9/q-55.php composed of millions of cells and each cell contains 46 chromosomes inside of its nuclei, which acts as the "brain" for the individual cell.

Of essajs chromosomes there are typically 2 sex chromosomes, if you are female you will have two X chromosomes, and if you are male you will have one X chromosome and one Y chromosome. When someone is diagnosed as having Triple X syndrome they have three X chromosomes, thus making it source disorder which effects females only.

Triple X syndrome is caused during the formation of reproductive cells eggs and sperm in one of the parents which is then passed down to their daughter. Research has discovered little about this disorder. Many girls and women who have the disorder may have no signs or symptoms. Symptoms that may be expressed include and may vary from, increased spacing between eyes, tall stature, a small head, delayed speech and language, delayed motor skills, seizures, delayed puberty, infertility, and rarely mental retardation.

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  • There is no cure for this disorder, and it is recommended to seek specialists in individual fields where the problem occurs, for example, see a speech and language pathologist if a delay in that area. There are medications to help with the symptoms.

    Tremors, rigidity movement, slowness of movement, instability, attention difficulties, memory loss, sleep problems, excessive sweating, and constipation and vision problems. Many neurodegenerative diseases are caused by genetic mutations. This essay will be discussing the similarities and differences learn more here the diseases of Sign Up Sign In.

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