DocSym
β
Searchsearch
Search
(Q98.5) Karyotype 47,xyy
More details coming soon
5 250 in individuals diagnosis karyotype 47,xyy confirmed
2 154 deaths with diagnosis karyotype 47,xyy
41% mortality rate associated with the disease karyotype 47,xyy
Diagnosis karyotype 47,xyy is diagnosed Men are 88.04% more likely than Women
4 936
Men receive the diagnosis karyotype 47,xyy
2 154 (43.6 %)Died from this diagnosis.
100
95
90
85
80
75
70
65
60
55
50
45
40
35
30
25
20
15
10
5
0
314
Women receive the diagnosis karyotype 47,xyy
0 (less than 0.1%)Died from this diagnosis.
Risk Group for the Disease karyotype 47,xyy - 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 karyotype 47,xyy
Absence or low individual and public risk
Karyotype 47,xyy - what does this mean
Karyotype 47,xyy is a chromosomal disorder caused by the presence of an extra y chromosome in each of a male's cells. it is the result of a nondisjunction event during meiosis in the father, resulting in a sperm cell with an extra y chromosome fertilizing an egg. this results in a male with 47 chromosomes instead of the normal 46.
What happens during the disease - karyotype 47,xyy
Karyotype 47,xyy is a chromosomal disorder caused by an extra copy of the y chromosome in males. this extra y chromosome results in an increased risk of learning disabilities, delayed development, and behavioral issues due to a disruption in the normal balance of hormones. additionally, males with this disorder are more likely to have tall stature, acne, and an increased risk of infertility.
Clinical Pattern
More details coming soon
How does a doctor diagnose
More details coming soon
Treatment and Medical Assistance
More details coming soon
14 Days of Hospitalization Required
28 Hours Required for Outpatient Treatment
Karyotype 47,xyy - Prevention
The prevention of karyotype 47,xyy is through genetic counseling and pre-natal screening. through genetic counseling, couples can be educated about the risks of having a child with this condition and be offered genetic testing to determine the chances of having a child with this condition. pre-natal screening can also be done to determine if the fetus has this condition.