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(O28.5) Abnormal chromosomal and genetic finding on antenatal screening of mother
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281 025 in individuals diagnosis abnormal chromosomal and genetic finding on antenatal screening of mother confirmed
Diagnosis abnormal chromosomal and genetic finding on antenatal screening of mother is diagnosed Prevalent in Women Only
0
Men receive the diagnosis abnormal chromosomal and genetic finding on antenatal screening of mother
0 (No mortality)Died from this diagnosis.
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281 025
Women receive the diagnosis abnormal chromosomal and genetic finding on antenatal screening of mother
0 (less than 0.1%)Died from this diagnosis.
Risk Group for the Disease abnormal chromosomal and genetic finding on antenatal screening of mother - Men aged 0 and Women aged 30-34
No Cases of the Disease Abnormal chromosomal and genetic finding on antenatal screening of mother identified in Men
Less common in men the disease occurs at Age 0-95+Less common in women the disease occurs at Age 0-9, 50-95+
In Women diagnosis is most often set at age 10-49
Disease Features abnormal chromosomal and genetic finding on antenatal screening of mother
Absence or low individual and public risk
Abnormal chromosomal and genetic finding on antenatal screening of mother - what does this mean
Abnormal chromosomal and genetic findings on antenatal screening of the mother can occur due to mutations in the mother's chromosomes or genes, which can be inherited or acquired. these mutations can cause various genetic disorders in the baby, such as down syndrome, turner syndrome, or klinefelter syndrome.
What happens during the disease - abnormal chromosomal and genetic finding on antenatal screening of mother
Abnormal chromosomal and genetic findings on antenatal screening of a mother can be caused by a variety of different factors, such as maternal age, genetic mutations, or environmental exposures. these findings can indicate an increased risk of genetic disorders or birth defects in the baby. diagnostic tests, such as amniocentesis or chorionic villus sampling, can be used to confirm the diagnosis and assess the severity of the condition. treatment and management of the condition will depend on the specific diagnosis and may include close monitoring of the pregnancy, surgery, or genetic counseling.
Clinical Pattern
More details coming soon
How does a doctor diagnose
- Ultrasound
- Amniocentesis
- Chorionic villus sampling (CVS)
- Fetal blood sampling
- Fetal skin biopsy
- Fluorescent in situ hybridization (FISH)
- Polymerase chain reaction (PCR)
- Karyotyping
Treatment and Medical Assistance
Main goal of the treatment: To treat the abnormal chromosomal and genetic finding on antenatal screening of mother.
- Provide genetic counseling
- Perform genetic testing to identify the cause of the abnormality
- Initiate prenatal diagnosis
- Refer to a specialist as needed
- Monitor the mother and baby throughout the pregnancy
- Provide support and guidance to the family
- Refer to a geneticist for further management
- Discuss the risks and benefits of available interventions
- Provide information about available resources
4 Days of Hospitalization Required
Average Time for Outpatient Care Not Established
Abnormal chromosomal and genetic finding on antenatal screening of mother - Prevention
The best way to prevent abnormal chromosomal and genetic findings on antenatal screening of the mother is to ensure that pregnant women receive adequate prenatal care, including regular check-ups and screenings. additionally, pregnant women should be educated about the risks of various genetic disorders and the importance of early detection. genetic counseling can also be beneficial in helping families to make informed decisions about their pregnancies.