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(Q98.0) Klinefelter syndrome karyotype 47,xxy
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5 250 in individuals diagnosis klinefelter syndrome karyotype 47,xxy confirmed
2 154 deaths with diagnosis klinefelter syndrome karyotype 47,xxy
41% mortality rate associated with the disease klinefelter syndrome karyotype 47,xxy
Diagnosis klinefelter syndrome karyotype 47,xxy is diagnosed Men are 88.04% more likely than Women
4 936
Men receive the diagnosis klinefelter syndrome karyotype 47,xxy
2 154 (43.6 %)Died from this diagnosis.
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Women receive the diagnosis klinefelter syndrome karyotype 47,xxy
0 (less than 0.1%)Died from this diagnosis.
Risk Group for the Disease klinefelter syndrome karyotype 47,xxy - Men and Women aged 0
In Men diagnosis is most often set at age 0-34, 45-54
Less common in men the disease occurs at Age 35-44, 55-95+Less common in women the disease occurs at Age 0-95+
In Women diagnosis is most often set at age 0-1
Disease Features klinefelter syndrome karyotype 47,xxy
Absence or low individual and public risk
Klinefelter syndrome karyotype 47,xxy - what does this mean
Klinefelter syndrome is a genetic disorder caused by the presence of an extra x chromosome in males, resulting in a karyotype of 47,xxy. it is the most common sex chromosome abnormality in males and can cause a variety of physical, cognitive, and psychological symptoms.
What happens during the disease - klinefelter syndrome karyotype 47,xxy
Klinefelter syndrome is a genetic disorder caused by the presence of an extra x chromosome in males. the extra x chromosome causes a disruption in the development of the testes, resulting in lower testosterone levels, which can lead to a variety of physical and psychological symptoms, including infertility, physical abnormalities, cognitive impairment, and behavioral issues. the extra x chromosome is caused by a process called nondisjunction, which occurs during the formation of sperm or egg cells, resulting in an abnormal number of chromosomes.
Clinical Pattern
More details coming soon
How does a doctor diagnose
- Physical examination
- Blood tests to measure hormone levels
- Chromosome analysis (karyotype)
- Ultrasound to look for testicular abnormalities
- Genetic testing to confirm a diagnosis of 47,XXY
Treatment and Medical Assistance
Main goal of the treatment: To reduce the symptoms of Klinefelter Syndrome and improve the quality of life of the patient.
- Monitoring of growth and development
- Treatment of associated medical conditions, such as obesity and diabetes
- Hormonal therapy to reduce the symptoms of hypogonadism
- Speech therapy to improve communication skills
- Occupational therapy to improve daily living skills
- Psychotherapy to address any emotional or behavioral problems
- Counseling and support for the patient and family
14 Days of Hospitalization Required
28 Hours Required for Outpatient Treatment
Klinefelter syndrome karyotype 47,xxy - Prevention
Klinefelter syndrome is a chromosomal disorder that cannot be prevented. however, early diagnosis and appropriate management of the condition can help reduce the severity of symptoms and improve quality of life. early diagnosis and treatment can help ensure that children with klinefelter syndrome receive appropriate educational and social support, as well as early intervention for any associated medical problems. it is also important to provide psychological support to individuals affected by the disorder.