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(O35.1) Maternal care for (suspected) chromosomal abnormality in fetus
More details coming soon
725 546 in individuals diagnosis maternal care for (suspected) chromosomal abnormality in fetus confirmed
Diagnosis maternal care for (suspected) chromosomal abnormality in fetus is diagnosed Prevalent in Women Only
0
Men receive the diagnosis maternal care for (suspected) chromosomal abnormality in fetus
0 (No mortality)Died from this diagnosis.
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725 546
Women receive the diagnosis maternal care for (suspected) chromosomal abnormality in fetus
0 (less than 0.1%)Died from this diagnosis.
Risk Group for the Disease maternal care for (suspected) chromosomal abnormality in fetus - Men aged 0 and Women aged 30-34
No Cases of the Disease Maternal care for (suspected) chromosomal abnormality in fetus 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, 55-69, 75-95+
In Women diagnosis is most often set at age 10-54, 70-74
Disease Features maternal care for (suspected) chromosomal abnormality in fetus
Absence or low individual and public risk
Maternal care for (suspected) chromosomal abnormality in fetus - what does this mean
Maternal care for a suspected chromosomal abnormality in the fetus may occur when an ultrasound scan or other prenatal testing indicates that the fetus may have an abnormal number of chromosomes. this can be caused by either an extra chromosome or a missing chromosome, and can lead to a variety of developmental issues in the infant.
What happens during the disease - maternal care for (suspected) chromosomal abnormality in fetus
Maternal care for a suspected chromosomal abnormality in the fetus is a complex process that involves the mother and her health care team. the mother must be evaluated for risk factors, such as advanced maternal age, family history, and previous pregnancy history. if a prenatal screening test suggests a chromosomal abnormality, then a diagnostic test, such as amniocentesis or chorionic villus sampling, can be performed to confirm the diagnosis. the mother must then be counseled on her options, such as prenatal diagnosis and management, termination of the pregnancy, or supportive care. she must also be supported emotionally and physically throughout the process.
Clinical Pattern
More details coming soon
How does a doctor diagnose
- Ultrasound
- Amniocentesis
- Chorionic Villus Sampling (CVS)
- Cell-free Fetal DNA Testing
- Fetal MRI
- Fetal Echocardiogram
- Fetal Blood Tests
Treatment and Medical Assistance
Main Goal: Provide maternal care for (suspected) chromosomal abnormality in fetus.
- Conduct a genetic screening test to confirm diagnosis.
- Educate the mother about the condition.
- Provide emotional and psychological support to the mother.
- Refer the mother to a specialist for further tests.
- Provide genetic counseling to the mother.
- Monitor the mother's health regularly.
- Provide nutritional advice to the mother.
- Refer the mother for genetic testing of the fetus.
- Provide information on prenatal care.
- Educate the mother on the risks and benefits of continuing the pregnancy.
- Refer the mother to a specialist in fetal medicine.
- Provide information on available treatments and support.
- Monitor the fetal development closely.
- Encourage the mother to make informed decisions about her pregnancy.
5 Days of Hospitalization Required
Average Time for Outpatient Care Not Established
Maternal care for (suspected) chromosomal abnormality in fetus - Prevention
Maternal care for suspected chromosomal abnormality in the fetus should include frequent ultrasounds to monitor fetal growth and development, genetic counseling to discuss the risks and benefits of prenatal testing, and referral to a specialist for further evaluation if necessary. additionally, pregnant women should be encouraged to receive regular prenatal care and follow a healthy lifestyle to reduce the risk of chromosomal abnormalities.