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(O35.2) Maternal care for (suspected) hereditary disease in fetus
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725 546 in individuals diagnosis maternal care for (suspected) hereditary disease in fetus confirmed
Diagnosis maternal care for (suspected) hereditary disease in fetus is diagnosed Prevalent in Women Only
0
Men receive the diagnosis maternal care for (suspected) hereditary disease in fetus
0 (No mortality)Died from this diagnosis.
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725 546
Women receive the diagnosis maternal care for (suspected) hereditary disease in fetus
0 (less than 0.1%)Died from this diagnosis.
Risk Group for the Disease maternal care for (suspected) hereditary disease in fetus - Men aged 0 and Women aged 30-34
No Cases of the Disease Maternal care for (suspected) hereditary disease 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) hereditary disease in fetus
Absence or low individual and public risk
Maternal care for (suspected) hereditary disease in fetus - what does this mean
Maternal care for (suspected) hereditary disease in fetus occurs when a pregnant woman carries a fetus that may have inherited a genetic disorder from one or both of its parents. this can be determined through family history, prenatal screening tests, and genetic testing. depending on the results, the mother may need to receive additional care during her pregnancy to help ensure the health of her baby.
What happens during the disease - maternal care for (suspected) hereditary disease in fetus
Maternal care for a suspected hereditary disease in a fetus is a complex process that involves both genetic and environmental factors. the genetic component involves a mutation in the genetic material of the fetus that is inherited from one or both parents, while the environmental component involves the mother's exposure to certain environmental factors, such as drugs or toxins, that can increase the risk of the fetus developing the disease. the mother's care for the fetus is essential in helping to identify any potential hereditary diseases and to provide treatment and support if needed.
Clinical Pattern
More details coming soon
How does a doctor diagnose
- Ultrasound scan to detect any structural abnormalities
- Blood tests to check for genetic markers
- Amniocentesis to detect any chromosomal abnormalities
- Chorionic villus sampling to detect any genetic disorders
- Fetal echocardiogram to detect any heart defects
- Fetal MRI to detect any brain abnormalities
- Fetal karyotyping to detect any chromosomal abnormalities
- Fetal genetic testing to detect any genetic mutations
Treatment and Medical Assistance
Main Goal: To provide appropriate care for the fetus with suspected hereditary disease.
- Perform prenatal genetic screening tests
- Receive genetic counseling
- Obtain an ultrasound to monitor fetal growth and development
- Perform regular prenatal visits
- Undergo additional tests, such as amniocentesis, if necessary
- Receive appropriate medical care and treatment
- Receive support and counseling from a multidisciplinary team
- Make informed decisions about the pregnancy and delivery
5 Days of Hospitalization Required
Average Time for Outpatient Care Not Established
Maternal care for (suspected) hereditary disease in fetus - Prevention
Maternal care for (suspected) hereditary disease in fetus should include regular prenatal care to monitor the health of the fetus, genetic testing to detect any mutations that may be associated with the disease, and genetic counseling to discuss the risks and benefits of any recommended interventions.