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(Q99.9) Chromosomal abnormality, unspecified
More details coming soon
31 258 in individuals diagnosis chromosomal abnormality, unspecified confirmed
5 008 deaths with diagnosis chromosomal abnormality, unspecified
16% mortality rate associated with the disease chromosomal abnormality, unspecified
Diagnosis chromosomal abnormality, unspecified is diagnosed Women are 1.77% more likely than Men
15 353
Men receive the diagnosis chromosomal abnormality, unspecified
2 572 (16.8 %)Died from this diagnosis.
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Women receive the diagnosis chromosomal abnormality, unspecified
2 436 (15.3 %)Died from this diagnosis.
Risk Group for the Disease chromosomal abnormality, unspecified - 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 chromosomal abnormality, unspecified
Absence or low individual and public risk
Chromosomal abnormality, unspecified - what does this mean
Chromosomal abnormality, unspecified occurs when there is a change in the number or structure of chromosomes. this can occur due to errors during cell division, leading to an abnormal number of chromosomes or an abnormal arrangement of genetic material. chromosomal abnormality, unspecified can cause a range of health problems, depending on the type and severity of the abnormality.
What happens during the disease - chromosomal abnormality, unspecified
Chromosomal abnormality is a condition in which there is a change in the structure or number of chromosomes. this can be caused by a mutation in the dna sequence, an error during cell division, or exposure to environmental factors such as radiation or certain chemicals. these changes can affect the normal development of an individual, leading to birth defects, physical defects, and health problems.
Clinical Pattern
More details coming soon
How does a doctor diagnose
- Complete Blood Count (CBC)
- Karyotype Test
- Fluorescence in situ Hybridization (FISH)
- Chromosomal Microarray Analysis (CMA)
- Prenatal Diagnosis
- Chorionic Villus Sampling (CVS)
- Amniocentesis
Treatment and Medical Assistance
Main goal of the treatment: To reduce or eliminate the effects of the chromosomal abnormality.
- Provide genetic counseling to the patient and their family.
- Conduct a thorough physical examination of the patient.
- Perform a karyotype test to identify the chromosome abnormality.
- Perform other tests such as ultrasound, MRI, and CT scans to identify any physical abnormalities.
- Prescribe medications to reduce symptoms and improve quality of life.
- Refer the patient to other specialists for further treatment.
- Provide psychological support to the patient and their family.
- Provide education and information about the condition.
- Provide support for the patient in managing daily activities.
23 Days of Hospitalization Required
Average Time for Outpatient Care Not Established
Chromosomal abnormality, unspecified - Prevention
Chromosomal abnormality, unspecified, can be prevented through pre-pregnancy genetic counseling and screening of prospective parents for known genetic disorders. additionally, pregnant women should receive regular prenatal care to monitor for any potential chromosomal abnormalities.