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Fragile X Syndrome (also known as FXS) is a life-altering condition that causes intellectual frailty. Those affected are prone to behavioral and learning challenges and may have physical imperfections.
What else can I help you with?
Is fragile x like Autism?
no Added: Fragile X is like autism in that the condition can be a spectrum disorder, no or mild symptoms to severe symptoms. Fragile X is Genetic, the genetics of Autism are still being determined. Fragile X can be diagnosed any where by any doctor by a simple blood test, Autism is a subjective diagnosis based on evaluations and observations.
What are the symptoms of Fragile-X Syndrome?
Fragile X Syndrome (also known as FXS) is a life-altering condition that causes intellectual frailty. Those affected are prone to behavioral and learning challenges and may have physical imperfections.
When and by who was Fragile X Discovered?
Fragile x syndrome was first described in 1943 by J.Purdon Martin and Julia Bell whose family had eleven members with fragile x symptoms although they did not know the cause or have a name for the condition at this time. In 1969, Fragile x was first discovered under the microscope by a scientist called Herbert Lubs who discovered that one of the arms of the X chromosome in people with fragile x was constricted which gave it the appearance of being broken which is how the name 'fragile x' came about. In 1991 Verkerk identified the cause for transcriptional silencing of the gene Fmr-1, that encodes the protein FMRP.
Is fragile X syndrome fatal?
Yes, the highest age someone with Fragile X Syndrome was 32. Everyone under that experienced headaches and fevers before they died. When they experience these symptoms they eventually go through spontaneously combustion.
Does fragile X get worse?
No, fragile x syndrome is not progressive
What have studies demonstrated about men who are carriers of the fragile X gene?
may begin to show signs of tremor disorder, gait instability and memory impairment as they age. The higher prevalence of these symptoms among grandfathers of children with fragile x syndrome was noted
Is there a certain age for fragile x syndrome to occur?
Fragile X is a genetic abnormality which is inherited and individuals therefore have the condition from birth, although, depending on the severity of the symptoms it is often undetected until early childhood. The average age of diagnosis is 8 years old. If however, parents are known to be carriers of Fragile X, the child may be given a blood test early on which is used to diagnose fragile x.
Can animals get Fragile X syndrome?
Fragile X syndrome is a genetic condition primarily affecting humans and is caused by a mutation in the FMR1 gene on the X chromosome. While animals can exhibit similar behaviors or symptoms associated with intellectual disabilities, they do not develop Fragile X syndrome in the same way humans do. Research in animal models, particularly mice, has been conducted to better understand the disorder, but the genetic mechanisms and manifestations differ significantly across species. Therefore, animals do not get Fragile X syndrome as it is defined in humans.
Where on the X chromosome does Fragile X take place?
Fragile X is a result of a mutation in the FMR1 gene on the X chromosome.
What cause fragile X syndrome?
The fragile X syndrome is a genetic disorder caused by mutation of the FMR1 gene on the X chromosome.
What is the treatment for fragel x syndrome?
A treatment plan for fragile X syndrome is tailored to the patientâ??s specific needs. Common treatments are: special education, speech and language therapy, occupational therapy, and medication.
Is it possible to be mildly affected by fragile x disease i have simian palm creases along with overly flexible thumb joints.i can be very obbsessive too. it has been diagnosed in family members?
Yes, it is possible to be mildly affected by Fragile X syndrome, as its symptoms can vary widely in severity. Features like simian palm creases and hyperflexible joints may be associated with genetic conditions, including Fragile X. Additionally, obsessive behaviors can occur in individuals with the syndrome. Given your family history and symptoms, consulting a genetic counselor or healthcare professional could provide clarity and guidance.
