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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 can cause epidermolysis bullosa?
Epidermolysis bullosa is a genetic disorder caused by mutations in genes that help hold the layers of the skin together. These mutations result in fragile skin that is prone to blistering and tearing from minor friction or trauma.
What is an example of a genetic disorder that is caused by insertion of extra codons in the X sex chromosome?
Fragile X Syndrome
What is an example of a genetic disorder that is caused by insertion of extra codons of the X sex chromosome?
Fragile X Syndrome
What is an examples of a genetic disorder that is cause by insertion of extra codons in the X sex chromosome?
Fragile X Syndrome
What is an example of a genetic disorder that is caused by insertion of an extra codons in the X sex chromosome?
Fragile X Syndrome
What is an example of a genetic disorder that is caused by insertion of extra codons in x sex chromosome?
Fragile X Syndrome
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.
Is fragile x a x linked disorder?
Yes, Fragile X syndrome is an X-linked genetic disorder that causes a range of developmental problems. It is caused by a mutation in the FMR1 gene located on the X chromosome. The condition is more commonly seen in males than in females because they have only one X chromosome.
What are the symptoms of osteporosis?
abnormal loss of bony tissue resulting in fragile porous bones attributable to a lack of calcium; most common in postmenopausal women
Will a person with fragile x syndrome be able to live independently?
Fragile X, like autism, is a spectrum disorder, which could result in anything from mild learning disabilities to severe impairment. Individuals can live independently, with or without supports. I recommend the documentary "Living with Fragile X" if you have the opportunity to see it.
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
