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Fragile X Syndrome
Probability and chromosomal #
Prognosis
The chromosome affected by FXS is the X chromosome the disorder is caused due to a gene being inactive and not producing a necessary protein The likelihood of developing this trait is 1 in 400,000 in males and 1 in 800,000 in females
Since poeple with the trait suffer from depression and anxiety they can be given medication. they can also be given extra help to make up for and learning or disciplinary set backs, people with this trait can generally live a happy normal life.
Sources
https://ghr.nlm.nih.gov/condition/fragile-x-syndrome
https://fragilex.org/fragile-x/genetics-and-inheritance/
Fragile X Syndrome
FXS is caused by the FMR1 gene to be "turned off" in a certain area and causes a lack of FMRP proteins, with the individual lacking the protein causes FXS.
Symptoms of FXS
Problems with learning, social, and behavioral functions are common
Physical features include large ears and elongated face
Social anxiety and depression is common
Current research and Treatment
Child With FXS
X Chromosome affected with FXS
Studies utilizing breakthroughs within the past 10 years are now in human trials, this is not a cure but a improvement to the affected person and family.
physical rehabilitation treatment may be used to help with physical disabilities and medicine can be used for depression and anxiety. However no "cure" is released yet.