(O28.9) Abnormal finding on antenatal screening of mother, unspecified

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281 025 in individuals diagnosis abnormal finding on antenatal screening of mother, unspecified confirmed

Diagnosis abnormal finding on antenatal screening of mother, unspecified is diagnosed Prevalent in Women Only

0

Men receive the diagnosis abnormal finding on antenatal screening of mother, unspecified

0 (No mortality)

Died from this diagnosis.

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281 025

Women receive the diagnosis abnormal finding on antenatal screening of mother, unspecified

0 (less than 0.1%)

Died from this diagnosis.

Risk Group for the Disease abnormal finding on antenatal screening of mother, unspecified - Men aged 0 and Women aged 30-34

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No Cases of the Disease Abnormal finding on antenatal screening of mother, unspecified identified in Men
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Less common in men the disease occurs at Age 0-95+Less common in women the disease occurs at Age 0-9, 50-95+
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In Women diagnosis is most often set at age 10-49

Disease Features abnormal finding on antenatal screening of mother, unspecified

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Absence or low individual and public risk
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Abnormal finding on antenatal screening of mother, unspecified - what does this mean

Abnormal findings on antenatal screening of a mother can occur due to a variety of reasons, including genetic abnormalities, infections, and other medical conditions. depending on the specific abnormality, further testing may be necessary to determine the cause and the best course of action for the mother and her unborn child.

What happens during the disease - abnormal finding on antenatal screening of mother, unspecified

The pathogenesis of this disease is likely multi-factorial, involving genetic, environmental, and lifestyle factors. a mother may have an abnormal finding on antenatal screening due to an underlying genetic disorder, exposure to environmental toxins or infectious agents, or unhealthy lifestyle choices such as smoking or alcohol consumption. in some cases, the cause of the abnormal finding may be unknown.

Clinical Pattern

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How does a doctor diagnose

  • Review medical history of the mother
  • Perform physical examination of the mother
  • Order laboratory tests such as blood tests, urine tests, and imaging tests
  • Perform genetic testing to detect any genetic abnormalities
  • Conduct fetal ultrasound to assess the health of the fetus
  • Perform amniocentesis to determine any chromosomal abnormalities
  • Conduct chorionic villus sampling (CVS) to detect any genetic abnormalities
  • Perform maternal serum screening to detect any abnormality in the fetus
  • Consult with a specialist to determine the best course of action

Treatment and Medical Assistance

Main Goal: Treat the disease based on the abnormal finding on antenatal screening of mother, unspecified.
  • Order additional tests to determine the cause of the abnormal finding
  • Perform a physical examination
  • Prescribe medications, if necessary
  • Refer to a specialist, if needed
  • Provide counseling and support
  • Monitor the mother and baby during and after pregnancy
  • Provide education on the risks of the disease
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4 Days of Hospitalization Required
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Average Time for Outpatient Care Not Established

Abnormal finding on antenatal screening of mother, unspecified - Prevention

The best way to prevent abnormal findings on antenatal screening of a mother is for pregnant women to receive regular prenatal care, including ultrasounds and tests to screen for potential abnormalities. eating a healthy diet, exercising regularly, and avoiding harmful substances such as alcohol and drugs can also help to reduce the risk of abnormal findings on antenatal screening. additionally, speaking with a medical professional about any family history of genetic disorders can help to identify any potential risks.