Although there is no cure for Fragile X, intervention for these secondary effects may be required. For the more apparent behavioral characteristics, parents and teachers are the main influences in a Fragile X child's life. Consistency in teaching procedures and in behavior management, both at home and at school, is vitally important. .
COGNITIVE DEFICITS ASSOCIATED WITH FRAGILE X SYNDROME.
Approximately 2.5% of the general population is mentally disabled. Of the 2.5%, 40% of all nonspecific mental disabilities and 10% of all mental disabilities are caused by Fragile X syndrome. Since the suggestion that approximately 1 in 2,000 males are affected with the Fragile X syndrome a profile of specific physical characteristics, social and emotional behaviors, and unique intellectual deficits has gradually surfaced.
It has been recently concluded that the foremost diagnosis can be based on the detection of a mutation on the DNA level. The ability to distinguish between a permutation and a full mutation provides a greater prediction for the risk of being mentally disabled. Identification by DNA analysis is an effective and dependable test for the diagnosis of Fragile X syndrome after birth as well as for prenatal and genetic counseling purposes. It is now possible to determine male or female carriers of Fragile X mutation with high reliability.
Females with Fragile X are not usually mentally disabled. Females do, however, generally display mild to severe learning disabilities. Females that inherit the chromosome from their mother appear to have greater difficulty with communication, socialization, affect and thought processing than do females who inherited the chromosome from their father. On the other hand, Fragile X males are usually moderately to severely mentally disabled. Along with being mentally disabled, affected males have a tendency to be autistic, hyperactive, self-abusive, anxious and even possibly psychotic.
Fragile X is among one of these disorders. ... Without this protein needed for brain function, fragile X syndrome is triggered. ... So far the most promising method of treating fragile X, this involves relieving symptoms of fragile X with current medicines. ... In order to discover if one has fragile X syndrome a few options are available. ... However, in 1992 an accurate fragile X DNA test was created. ...
This Syndrome is usually inherited from one of the parents and about 30% of cases occur when the abnormal gene arises in an egg or a sperm of an unaffected parent.3 4 In diagnosing Marfan Syndrome, X-rays, slit-lamp eye examination, skeletal examination and complete family history are used. ... It becomes wider from being stretched thus becoming more fragile. ... A person with Marfan Syndrome. ... If the Syndrome is identified at birth, close monitoring of the skeleton is necessary, especially during adolescence. ... What would one rather have: Having an abortion after amniocente...
Autism has been found in children with brain abnormalities such as congenital rubella syndrome, neurofibromatosis, and tuberous sclerosis. Autism can also be present in genetic syndromes such as fragile X syndrome and phenylketonuria. ... Doctors will often discuss their medical history, such as possibility of seizures, hearing and visual impairments along with other conditions or syndromes such as fragile X syndrome. ... A test for fragile X syndrome may be given because of its direct association with autism. ...
Autism has been found in children with brain abnormalities such as congenital rubella syndrome, neurofibromatosis, and tuberous sclerosis. Autism can also be present in genetic syndromes such as fragile X syndrome and phenylketonuria. ... Doctors will often discuss their medical history, such as possibility of seizures, hearing and visual impairments along with other conditions or syndromes such as fragile X syndrome. ... A test for fragile X syndrome may be given because of its direct association with autism. ...
"Genetic causes include single-gene defects such as Fragile X syndrome and chromosomal disorders such as Down syndrome. Scientists in 1992 identified Fragile X syndrome as the most common inherited cause of mental retardation, responsible for up to 10 percent of cases. People with this condition inherit a defective gene that results in a weak spot on the X chromosome, a sex chromosome. ... Fragile X syndrome is more likely to cause retardation in males than females. ... Down syndrome occurs when people inherit all or part of an extra copy of a pair of chromosomes known together as chromoso...
As a Biology major, my career options are plentiful. I have always known that I wanted to help people, and I have always been interested in the medical field. I could never become a doctor or a nurse, because of my fear of blood and needles; therefore, I am seriously considering occupational thera...
One major cause of these impairments can stem from a child diagnosed with a Syndrome. "A Syndrome is identified when a certain number of features co-occur across individuals." (Pg.74) A few examples of Syndromes that can cause problems in speech sound production are Fetal Alcohol Syndrome, Down Syndrome, Velocardiofacial Syndrome, Genetic Syndromes, such as Fragile X Syndrome, and Chromosomal Syndromes, such as Turner Syndrome, Pierre Robin, Cri du chat, Klinefelter, and DiGeorge Syndrome. The effects of most of these Syndromes include Hearing Loss, Language Delay, Mental Retardation...
Although X-ray machines have been the chief mechanical tools for internal observations of the human body since Wilhelm Roentgen discovered X-rays in 1901, the development of computers made it possible for better and more accurate techniques to be applied to scan the human body. ... This method of scanning generally involves X-rays and enables scientists to view the inside of the head in a three dimensional format on a computer screen. ... Their observations lead to a hypothesis which stated that if Thrombin is released from the blood stream into the fragile cavities between brain cel...
