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(Q99.2) Fragile x chromosome
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31 258 in individuals diagnosis fragile x chromosome confirmed
5 008 deaths with diagnosis fragile x chromosome
16% mortality rate associated with the disease fragile x chromosome
Diagnosis fragile x chromosome is diagnosed Women are 1.77% more likely than Men
15 353
Men receive the diagnosis fragile x chromosome
2 572 (16.8 %)Died from this diagnosis.
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15 905
Women receive the diagnosis fragile x chromosome
2 436 (15.3 %)Died from this diagnosis.
Risk Group for the Disease fragile x chromosome - Men and Women aged 0
In Men diagnosis is most often set at age 0-34, 60-64, 70-74
Less common in men the disease occurs at Age 35-59, 65-69, 75-95+Less common in women the disease occurs at Age 5-9, 30-34, 45-49, 55-59, 65-95+
In Women diagnosis is most often set at age 0-5, 10-29, 35-44, 50-54, 60-64
Disease Features fragile x chromosome
Absence or low individual and public risk
Fragile x chromosome - what does this mean
Fragile x chromosome is a genetic disorder caused by a mutation of the x chromosome, which affects the development of the brain and can result in intellectual disability, behavioral and learning challenges, and physical characteristics. it is one of the most common causes of inherited intellectual disability and is the most common known single gene cause of autism spectrum disorder.
What happens during the disease - fragile x chromosome
Fragile x chromosome is a genetic disorder caused by an abnormality on the x chromosome. it is caused by a mutation in the fmr1 gene which prevents the production of a protein necessary for normal development. this mutation results in an abnormally expanded section of the x chromosome, which can lead to a wide range of physical, cognitive, and behavioral symptoms.
Clinical Pattern
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How does a doctor diagnose
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Treatment and Medical Assistance
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23 Days of Hospitalization Required
Average Time for Outpatient Care Not Established
Fragile x chromosome - Prevention
Fragile x chromosome is a genetic condition that can be prevented by pre-conception genetic counseling and testing for carriers of the fragile x mutation. couples at risk for having a child with fragile x should seek genetic counseling to determine their risk and to discuss available options.