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(O28) Abnormal findings on antenatal screening of mother
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281 025 in individuals diagnosis abnormal findings on antenatal screening of mother confirmed
Diagnosis abnormal findings on antenatal screening of mother is diagnosed Prevalent in Women Only
0
Men receive the diagnosis abnormal findings on antenatal screening of mother
0 (No mortality)Died from this diagnosis.
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281 025
Women receive the diagnosis abnormal findings on antenatal screening of mother
0 (less than 0.1%)Died from this diagnosis.
Risk Group for the Disease abnormal findings on antenatal screening of mother - Men aged 0 and Women aged 30-34
No Cases of the Disease Abnormal findings 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 findings on antenatal screening of mother
Absence or low individual and public risk
Abnormal findings on antenatal screening of mother - what does this mean
Abnormal findings on antenatal screening of mothers can occur due to a variety of reasons, including genetic abnormalities in the fetus, infections, and problems with the placenta. these abnormalities can be detected through a variety of tests, including ultrasound, blood tests, and amniocentesis. depending on the type of abnormality, a doctor may recommend further testing or treatments to help ensure the health of the mother and baby.
What happens during the disease - abnormal findings on antenatal screening of mother
Abnormal findings on antenatal screening of the mother can be caused by a variety of underlying conditions, including genetic abnormalities, infections, and other medical conditions. these conditions can lead to a wide range of symptoms and complications, including preterm labor, low birth weight, and birth defects. the exact cause of the abnormal findings can be determined through further testing and evaluation, such as genetic testing, imaging studies, and laboratory tests. treatment and management of the underlying condition can help to reduce the risk of complications for the mother and the baby.
Clinical Pattern
More details coming soon
How does a doctor diagnose
- Perform a physical examination of the mother and fetus.
- Order laboratory tests such as complete blood count, urine analysis, and blood tests to check for infections, hormones, and genetic markers.
- Perform imaging studies such as ultrasound, MRI, and/or CT scan to assess fetal anatomy and development.
- Order genetic tests such as amniocentesis or chorionic villus sampling (CVS) to identify any chromosomal abnormalities.
- Perform non-invasive prenatal testing (NIPT) to screen for any genetic conditions.
- Refer to a specialist for further evaluation and management.
Treatment and Medical Assistance
Main Goal of the Treatment: To effectively treat the abnormal findings on antenatal screening of the mother.
- Consultation with an obstetrician and genetic counselor.
- Detailed ultrasound scan of the fetus.
- Maternal blood tests to identify any chromosomal abnormalities.
- Amniocentesis to obtain fetal cells for chromosomal analysis.
- Chorionic villus sampling to obtain fetal cells for chromosomal analysis.
- Follow-up monitoring of the pregnancy.
- Regular antenatal check-ups.
- Nutritional advice for the mother.
- Emotional support for the mother.
4 Days of Hospitalization Required
Average Time for Outpatient Care Not Established
Abnormal findings on antenatal screening of mother - Prevention
Abnormal findings on antenatal screening of the mother can be prevented through regular visits to the doctor throughout pregnancy, eating a balanced diet, taking prenatal vitamins, avoiding alcohol, drugs, and smoking, and getting regular exercise.