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(Q98.8) Other specified sex chromosome abnormalities, male phenotype
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5 250 in individuals diagnosis other specified sex chromosome abnormalities, male phenotype confirmed
2 154 deaths with diagnosis other specified sex chromosome abnormalities, male phenotype
41% mortality rate associated with the disease other specified sex chromosome abnormalities, male phenotype
Diagnosis other specified sex chromosome abnormalities, male phenotype is diagnosed Men are 88.04% more likely than Women
4 936
Men receive the diagnosis other specified sex chromosome abnormalities, male phenotype
2 154 (43.6 %)Died from this diagnosis.
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Women receive the diagnosis other specified sex chromosome abnormalities, male phenotype
0 (less than 0.1%)Died from this diagnosis.
Risk Group for the Disease other specified sex chromosome abnormalities, male phenotype - 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 other specified sex chromosome abnormalities, male phenotype
Absence or low individual and public risk
Other specified sex chromosome abnormalities, male phenotype - what does this mean
Other specified sex chromosome abnormalities, male phenotype is a genetic disorder caused by a chromosomal abnormality in which a male has at least one extra x chromosome in addition to the normal xy chromosome pair, resulting in a genotype of xxy. this can lead to infertility, delayed puberty, and physical differences such as tall stature, and learning and behavioral problems.
What happens during the disease - other specified sex chromosome abnormalities, male phenotype
Other specified sex chromosome abnormalities, male phenotype is caused by the presence of an abnormal number of sex chromosomes. these abnormalities can include having an extra or missing x or y chromosome, or having a combination of both. these abnormalities can lead to a range of physical and mental health issues, including infertility, learning disabilities, and physical malformations.
Clinical Pattern
More details coming soon
How does a doctor diagnose
- Physical examination
- Karyotype analysis
- Chromosome analysis
- Genetic testing
- Hormone testing
- Ultrasound of reproductive organs
- X-ray of the skeletal system
- Blood tests
- Urine tests
Treatment and Medical Assistance
Main Goal: To treat Other specified sex chromosome abnormalities, male phenotype.
- Identify the underlying cause of the disorder
- Perform genetic testing to confirm the diagnosis
- Provide counseling for the patient and their family
- Provide hormone replacement therapy
- Monitor the patient's growth and development
- Provide regular physical exams
- Monitor for any complications or side effects
- Provide psychological support and counseling
- Refer to specialists as needed
14 Days of Hospitalization Required
28 Hours Required for Outpatient Treatment
Other specified sex chromosome abnormalities, male phenotype - Prevention
The best way to prevent other specified sex chromosome abnormalities, male phenotype is to ensure that all pregnant women receive regular prenatal care. this includes receiving genetic counseling and testing, as well as being aware of the potential risk factors associated with this condition, such as advanced maternal age and family history. additionally, women should be encouraged to make healthy lifestyle choices, such as avoiding tobacco, alcohol, and illicit drugs, to reduce the risk of this condition.