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(Q92.9) Trisomy and partial trisomy of autosomes, unspecified
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6 330 in individuals diagnosis trisomy and partial trisomy of autosomes, unspecified confirmed
3 107 deaths with diagnosis trisomy and partial trisomy of autosomes, unspecified
49% mortality rate associated with the disease trisomy and partial trisomy of autosomes, unspecified
Diagnosis trisomy and partial trisomy of autosomes, unspecified is diagnosed Women are 46.76% more likely than Men
1 685
Men receive the diagnosis trisomy and partial trisomy of autosomes, unspecified
1 969 (116.9 %)Died from this diagnosis.
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Women receive the diagnosis trisomy and partial trisomy of autosomes, unspecified
1 138 (24.5 %)Died from this diagnosis.
Risk Group for the Disease trisomy and partial trisomy of autosomes, unspecified - Men and Women aged 0
In Men diagnosis is most often set at age 0-9
Less common in men the disease occurs at Age 10-95+Less common in women the disease occurs at Age 5-9, 20-24, 40-95+
In Women diagnosis is most often set at age 0-5, 10-19, 25-39
Disease Features trisomy and partial trisomy of autosomes, unspecified
Absence or low individual and public risk
Trisomy and partial trisomy of autosomes, unspecified - what does this mean
Trisomy and partial trisomy of autosomes, unspecified, is a genetic disorder in which an individual has three copies of an autosomal chromosome instead of the usual two. this can occur in any of the autosomal chromosomes and can cause a variety of physical and mental developmental delays and disabilities.
What happens during the disease - trisomy and partial trisomy of autosomes, unspecified
Trisomy and partial trisomy of autosomes is a chromosomal disorder caused by an extra or partial copy of an autosome. this can be caused by either a meiotic or mitotic error, such as nondisjunction, or by a chromosomal rearrangement, such as an inversion or translocation. this can lead to a variety of health problems, including developmental delays, physical abnormalities, and intellectual disabilities.
Clinical Pattern
More details coming soon
How does a doctor diagnose
- Physical examination
- Chromosomal analysis
- Cytogenetic analysis
- Fluorescent in situ hybridization (FISH) test
- Karyotyping
- Molecular genetic testing
- Ultrasound
- Amniocentesis
- Chorionic villus sampling (CVS)
Treatment and Medical Assistance
Main goal of the treatment: To reduce the symptoms of trisomy and partial trisomy of autosomes, unspecified.
- Perform genetic counseling and testing.
- Provide appropriate medical care and treatment.
- Develop an individualized treatment plan.
- Provide emotional support to the patient and family.
- Administer medications to reduce symptoms and improve quality of life.
- Refer patient to specialists, as needed.
- Monitor and assess the patient's progress.
- Educate patient and family about the condition.
- Provide physical, occupational, and/or speech therapy.
- Provide nutritional counseling.
13 Days of Hospitalization Required
Average Time for Outpatient Care Not Established
Trisomy and partial trisomy of autosomes, unspecified - Prevention
Trisomy and partial trisomy of autosomes, unspecified can be prevented by avoiding exposure to environmental toxins, maintaining a healthy lifestyle with a balanced diet and regular exercise, and reducing stress levels. genetic counseling and prenatal testing can also help to identify any potential risks of trisomy or partial trisomy before birth.