Fragile X Syndrome, Sample of Essays.

Fragile X syndrome is the result of a single gene mutation, a mutation of the FMR1 gene, located on the X chromosome. Every person has 23 pairs of chromosomes (46 individual chromosomes). Twenty two pairs of chromosomes are autosomes and one pair is an allosome, also known as sex the chromosomes.

Understanding the genetics of Fragile X Syndrome is the key to understanding why girls and boys differ in degree of learning disability. Research suggests.

Introduction Fragile X syndrome is the most common cause of inherited mental retardation, seen in approximately one in 1,200 males and one in 2,500 females. Males with fragile X syndrome usually have mental retardation and often exhibit characteristic physical features and behavior (Hagerma.

Fragile X Syndrome, also known as Martin-Bell Syndrome or Escalante Syndrome, is a genetic syndrome which manifests in a wide range of physical, intellectual, emotional, StudentShare Our website is a unique platform where students can share their papers in a matter of giving an example of the work to be done.

Fragile X syndrome is caused by mutants in the FMR1 cistron, which is located on the X chromosome. More specifically, it is caused by an expanded repeat of the CGG three in the cistron. In a normal individual, the section repeats approximately 5 to 40 times, but in people with the syndrome, the three is repeated more than 200 times, doing the FMR1 cistron to be silenced.

This essay has been submitted by a student. This is not an example of the work written by professional essay writers. Everything You Need to Know About Fragile X Syndrome: Symptoms, Causes, Risks, Diagnosis, Treatment.

Introduction Fragile X syndrome is the most common cause of inherited mental retardation, seen in approximately one in 1,200 males and one in 2,500 females. Males with fragile X syndrome usually have mental retardation and often exhibit characteristic physical features and behavior (Hagerman and Silverman, 1991; Warren and Nelson, 1994).

Understanding Fragile X Syndrome Essay example - Fragile-X Associated Disorders Information and facts for families, patients and health care providers. How common is Fragile X. Fragile X syndrome is the most common inherited cause of intellectual disabilities and the most common known cause of autism. Fragile X affects 1 in 4000 males and 1 in.

Fragile X syndrome results from a mutation in the FMR1 gene, which is on the X chromosome. There are currently no treatments or cures for fragile X syndrome. The best that medical science can offer are medications for various symptoms, attempting to minimize the secondary characteristics of the disease, such as anxiety, ADHD, hypersensitivity, and problems with working memory.

Title. Complications and investigations of Fragile X syndrome. Introduction. Fragile X syndrome is considered the most common heritable form of mental retardation, it affects approximately 1 in 4000 males and 1 in 8000 female it is an X linked disease caused by mutation in the” FMR1 gene “This mutation in dynamic it varies in length and so in severity from generation to generation The.

This paper discusses the complexities and mysteries surrounding fragile X syndrome. After explaining that fragile X syndrome is a serious genetic disorder that is believed to be the most common form of inherited metal impairment, the paper then attempts to clear up the confusion and misconceptions that surround the syndrome.

Fragile X Syndrome research papers discuss the genetic condition that is marked by an inherited intellectual disability. Fragile X syndrome (FXS) is a genetic condition, marked by inherited intellectual disability, especially in boys. About half of all children diagnosed with fragile X syndrome also meet criteria for autism spectrum disorder.