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  1. Fetal cause: Fetal malformations, fetus swallowing amniotic fluid.
  2. Genetic abnormalities: Abnormal number of chromosomes.
  3. Cardiovascular defects: Heart diseases, shortness of breath, chest pain.
  4. Neural tube defects: Conditions like anencephaly and open Spina Bifida.
  5. Maternal cause: Uncontrolled diabetes in the mother, increase in fetal blood sugar, kidney problems.
  6. Carrying twins or triplets: Multiple pregnancies occur in 8–10% of women.
  7. Anemia: Fetal anemia cases in 1–11 of cases.
  8. Viral infections: Parvovirus B19, rubella, cytomegalovirus.
  1. Breathlessness while lying down
  2. Palpitation
  3. Larger abdomen
  4. Heartburn
  5. Constipation
  6. Pressure in belly
  7. Swollen feets
  8. Weight gain
  1. Ultrasound: Polyhydramnios is detected using two methods of ultrasound: Amniotic fluid index and single deepest pocket.
  2. Blood tests: The blood test includes testing of ABO and Rh blood grouping and measuring the sugar levels.
  3. Laboratory tests: The laboratory tests include several screenings like blood glucose, maternal infection, etc.
  4. Fluid test: The fluid test is carried out to make the estimation of alpha-fetoprotein.

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