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(Q97.0) Karyotype 47,xxx
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4 436 in individuals diagnosis karyotype 47,xxx confirmed
620 deaths with diagnosis karyotype 47,xxx
14% mortality rate associated with the disease karyotype 47,xxx
Diagnosis karyotype 47,xxx is diagnosed Prevalent in Women Only
0
Men receive the diagnosis karyotype 47,xxx
0 (No mortality)Died from this diagnosis.
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4 436
Women receive the diagnosis karyotype 47,xxx
620 (14.0 %)Died from this diagnosis.
Risk Group for the Disease karyotype 47,xxx - Men aged 0 and Women aged 15-19
No Cases of the Disease Karyotype 47,XXX identified in Men
Less common in men the disease occurs at Age 0-95+Less common in women the disease occurs at Age 5-9, 30-39, 55-95+
In Women diagnosis is most often set at age 0-5, 10-29, 40-54
Disease Features karyotype 47,xxx
Absence or low individual and public risk
Karyotype 47,xxx - what does this mean
Karyotype 47,xxx is a chromosomal abnormality that occurs when a female has an extra x chromosome, resulting in a total of 47 chromosomes instead of the usual 46. this condition is also known as triple x syndrome, and can cause developmental delays, learning disabilities, and physical differences such as tall stature and weak muscle tone.
What happens during the disease - karyotype 47,xxx
Karyotype 47,xxx is a chromosomal disorder caused by the presence of an extra x chromosome in a female's cells, resulting in a total of 47 chromosomes instead of the normal 46. this extra x chromosome can cause a range of physical, developmental, and mental health issues, including infertility, learning disabilities, and behavioral problems. it can also cause a variety of physical features, such as a tall stature, a webbed neck, and a low hairline.
Clinical Pattern
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How does a doctor diagnose
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Treatment and Medical Assistance
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7 Days of Hospitalization Required
Average Time for Outpatient Care Not Established
Karyotype 47,xxx - Prevention
Prevention of karyotype 47,xxx involves early identification of the disorder through prenatal testing and genetic counseling. genetic counseling can help couples understand their risks of having a child with this disorder and provide information on available options for family planning. additionally, couples can consider preimplantation genetic diagnosis (pgd) to screen embryos for karyotype 47,xxx before implantation.