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(Q95.1) Chromosome inversion in normal individual
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3 714 in individuals diagnosis chromosome inversion in normal individual confirmed
1 384 deaths with diagnosis chromosome inversion in normal individual
37% mortality rate associated with the disease chromosome inversion in normal individual
Diagnosis chromosome inversion in normal individual is diagnosed Women are 51.80% more likely than Men
895
Men receive the diagnosis chromosome inversion in normal individual
0 (less than 0.1%)Died from this diagnosis.
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2 819
Women receive the diagnosis chromosome inversion in normal individual
1 384 (49.1 %)Died from this diagnosis.
Risk Group for the Disease chromosome inversion in normal individual - Men aged 0 and Women aged 10-14
In Men diagnosis is most often set at age 0-1, 15-19, 65-69
Less common in men the disease occurs at Age 0-14, 20-64, 70-95+Less common in women the disease occurs at Age 5-9, 15-19, 30-44, 50-59, 65-74, 80-95+
In Women diagnosis is most often set at age 0-5, 10-14, 20-29, 45-49, 60-64, 75-79
Disease Features chromosome inversion in normal individual
Absence or low individual and public risk
Chromosome inversion in normal individual - what does this mean
Chromosome inversion in normal individuals occurs when a chromosome breaks and reattaches in the opposite direction, resulting in a reversed piece of genetic material. this can cause genetic mutations, which can lead to conditions such as birth defects, infertility, or other health issues.
What happens during the disease - chromosome inversion in normal individual
Chromosome inversion in a normal individual is caused by a break in the chromosome in the cell's nucleus, followed by the chromosome pieces being reattached in a reverse orientation. this can occur spontaneously or be triggered by environmental factors such as radiation or certain chemicals. the inversion can cause genetic mutations, which may lead to changes in the individual's phenotype.
Clinical Pattern
More details coming soon
How does a doctor diagnose
- Physical examination
- Chromosomal analysis
- Genetic testing
- Ultrasound imaging
- Blood tests
- CT scan
- MRI scan
Treatment and Medical Assistance
Main goal of treatment: To reduce the risk of complications caused by chromosome inversion in a normal individual.
- Conduct genetic counseling to understand the implications of the inversion.
- Ensure regular follow-up appointments with a medical professional.
- Undergo genetic testing to determine the exact type of inversion.
- Monitor for any physical or mental developmental delays.
- Take necessary precautions to prevent any potential complications from the inversion.
- Opt for fertility treatments if the individual is trying to conceive.
- Undergo regular screening for any potential complications.
- Ensure the individual is up-to-date on all vaccinations.
- Manage any associated medical conditions.
6 Days of Hospitalization Required
26 Hours Required for Outpatient Treatment
Chromosome inversion in normal individual - Prevention
Chromosome inversion in normal individuals can be prevented by genetic counseling, which can help individuals understand the risks associated with the condition and make informed decisions about having children. additionally, prenatal screening and testing can help detect chromosome inversion in a fetus and provide options for couples who may be at risk of having a child with the condition.