A standard, specialized ultrasound called a nuchal translucency screening is done between weeks 11 and 13 of pregnancy. Increased fluid near the nuchal fold, the area at the base of the neck, in fetuses may indicate a genetic issue like Down syndrome. Since nuchal translucency is a prenatal test, the results can only provide statistical evidence rather than a definitive answer regarding your child's chromosomal condition. To provide further information about the likelihood that your child may be born with a genetic condition, it is frequently paired with a blood test. An ultrasound performed in the first trimester to assess your baby's risk of Down syndrome and certain other chromosomal abnormalities is called the NT + NB scan (Nuchal transluceny & Nasal Bone scan).
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