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(Q99.8) Other specified chromosome abnormalities
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31 258 in individuals diagnosis other specified chromosome abnormalities confirmed
5 008 deaths with diagnosis other specified chromosome abnormalities
16% mortality rate associated with the disease other specified chromosome abnormalities
Diagnosis other specified chromosome abnormalities is diagnosed Women are 1.77% more likely than Men
15 353
Men receive the diagnosis other specified chromosome abnormalities
2 572 (16.8 %)Died from this diagnosis.
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15 905
Women receive the diagnosis other specified chromosome abnormalities
2 436 (15.3 %)Died from this diagnosis.
Risk Group for the Disease other specified chromosome abnormalities - Men and Women aged 0
In Men diagnosis is most often set at age 0-34, 60-64, 70-74
Less common in men the disease occurs at Age 35-59, 65-69, 75-95+Less common in women the disease occurs at Age 5-9, 30-34, 45-49, 55-59, 65-95+
In Women diagnosis is most often set at age 0-5, 10-29, 35-44, 50-54, 60-64
Disease Features other specified chromosome abnormalities
Absence or low individual and public risk
Other specified chromosome abnormalities - what does this mean
Other specified chromosome abnormalities occur when there is an atypical number or structure of chromosomes, which can be caused by a variety of factors such as errors during cell division, environmental factors, or genetic mutations. these abnormalities can lead to a variety of symptoms and can be diagnosed through genetic testing.
What happens during the disease - other specified chromosome abnormalities
Other specified chromosome abnormalities is a condition where there is an abnormality in the number or structure of chromosomes, which can be caused by a variety of factors, such as abnormal cell division during meiosis, exposure to radiation, or exposure to certain chemicals. this can lead to a range of genetic disorders, including intellectual disability, physical malformations, and infertility.
Clinical Pattern
Other specified chromosome abnormalities is a group of genetic disorders caused by an abnormal number of chromosomes or a structural abnormality in one or more chromosomes. This can include missing, extra, or rearranged chromosomes. Symptoms vary depending on the specific abnormality present, but can include developmental delays, intellectual disability, physical malformations, and other physical and mental health problems. Diagnosis is typically done through genetic testing. Treatment may include medication, physical and occupational therapy, and genetic counseling.
How does a doctor diagnose
- Collect a complete medical history.
- Perform a physical examination.
- Order a karyotype test.
- Order a chromosomal microarray analysis.
- Order a fluorescent in situ hybridization (FISH) test.
- Order a quantitative PCR (qPCR) test.
- Order a high-resolution array comparative genomic hybridization (aCGH) test.
- Order a targeted gene panel for chromosome abnormalities.
Treatment and Medical Assistance
Main goal of the treatment: To reduce the symptoms and improve the quality of life of the patient with Other Specified Chromosome Abnormalities.
- Provide genetic counseling to the patient and family.
- Perform regular physical examinations to monitor the patient's condition.
- Provide psychosocial support to the patient and family.
- Prescribe medications to manage symptoms.
- Refer the patient to a specialist for further evaluation.
- Refer the patient to physical, occupational, and speech therapy, if needed.
- Provide dietary and lifestyle advice to the patient.
- Provide education and support to the patient and family.
- Perform genetic testing to confirm diagnosis.
- Refer the patient to a genetic counselor for further genetic testing and counseling.
23 Days of Hospitalization Required
Average Time for Outpatient Care Not Established
Other specified chromosome abnormalities - Prevention
The best way to prevent other specified chromosome abnormalities is to ensure that all women of childbearing age receive regular medical check-ups and screenings. additionally, pregnant women should receive prenatal care to ensure that any chromosomal abnormalities can be detected as early as possible. genetic counseling is also recommended for those at risk of passing on chromosomal abnormalities to their children.