The triple marker test is a useful diagnostic tool that helps identify chromosomal abnormalities of an unborn child. It helps to identify any congenital disabilities priorly and resolve the condition. It is usually performed in the second trimester of pregnancy.
Hi, Welcome to icliniq.com. It is done to screen for the possibility of certain birth defects in the baby, like Down's syndrome, abnormalities of the brain and spinal cord.
Hello, Welcome to icliniq.com. I have seen your reports. (attachment removed to protect patient identity). During the first scan, your baby was 11 weeks and the NT (nuchal translucency) was 3.17.
Hi, Welcome to icliniq.com. Please send a clear photograph, which can be readable. This report (attachment removed to protect patient identity) is regarding the risk of Down syndrome in a fetus.
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