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Replying to @jewlyaah Trisomy 18 is a genetic condition where there are three copies of chromosome 18 instead of two. Unfortunately the majority of babies who are diagnosed with this condition will pass within the first few days of being born. On ultrasound, we usually suspect T18 on the anatomy scan in the second trimester if we see certain characteristics like clench fists, a symmetrically small baby with increased amniotic fluid, choroid plexus cysts, a cleft lip or palate or heart defects. #
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Replying to @mackfitz96 Monosomy 18 results from a missing chromosome 18, so instead of having two copies of chromosome 18, there is only one. This genetic condition is difficult to diagnose using ultrasound alone and it's usually a combination of NIPT bloodwork prenatal testing and ultrasound or diagnosis after birth that detects this condition. Sometimes holoprosencephaly, a thickened nuchal translucency or facial defects can be seen on ultrasound with Monosomy 18. #greenscreen #ultrasound #ul
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