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(Q95.0) Balanced translocation and insertion in normal individual
More details coming soon
3 714 in individuals diagnosis balanced translocation and insertion in normal individual confirmed
1 384 deaths with diagnosis balanced translocation and insertion in normal individual
37% mortality rate associated with the disease balanced translocation and insertion in normal individual
Diagnosis balanced translocation and insertion in normal individual is diagnosed Women are 51.80% more likely than Men
895
Men receive the diagnosis balanced translocation and insertion in normal individual
0 (less than 0.1%)Died from this diagnosis.
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2 819
Women receive the diagnosis balanced translocation and insertion in normal individual
1 384 (49.1 %)Died from this diagnosis.
Risk Group for the Disease balanced translocation and insertion 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 balanced translocation and insertion in normal individual
Absence or low individual and public risk
Balanced translocation and insertion in normal individual - what does this mean
A balanced translocation and insertion in a normal individual occurs when there is an exchange of genetic material between two chromosomes or when a small chromosome piece is inserted into one of the chromosomes. this exchange or insertion does not cause any genetic abnormalities, and the individual remains healthy.
What happens during the disease - balanced translocation and insertion in normal individual
Balanced translocation and insertion is a genetic condition in which a segment of dna is moved from one chromosome to another, or inserted into a chromosome, without any genetic material being lost or gained. this condition is typically asymptomatic in the individual, but can cause issues in the production of proteins and can lead to an increased risk of developing certain diseases.
Clinical Pattern
More details coming soon
How does a doctor diagnose
- Physical examination
- Blood tests
- Imaging tests (such as X-rays, MRI, CT scans, or ultrasound)
- Genetic testing
- Cytogenetic testing
- Fluorescence in situ hybridization (FISH)
- Chromosome analysis
- Prenatal testing
Treatment and Medical Assistance
Main goal: Treating the disease of Balanced translocation and insertion in normal individual
- Identifying the disease and its symptoms
- Performing genetic testing to confirm the diagnosis
- Developing a personalized treatment plan based on the individual's medical history and lifestyle
- Monitoring the patient's response to treatment and adjusting the plan accordingly
- Providing counseling and support to the patient and their family
- Referring the patient to specialists for additional treatment or support
- Providing ongoing follow-up to evaluate the patient's progress
6 Days of Hospitalization Required
26 Hours Required for Outpatient Treatment
Balanced translocation and insertion in normal individual - Prevention
Balanced translocation and insertion in normal individuals can be prevented by avoiding activities that may cause chromosomal damage, such as exposure to radiation and certain chemicals, and by maintaining a healthy lifestyle, including eating a balanced diet, exercising regularly, and avoiding smoking and excessive alcohol consumption.