VP34.02: Use of the focus point for plane acquisition to improve reproducibility in fetal biometry

Abstract

Virtual poster abstracts the fetus was noted to be homozygous for both parental pathogenic mutations. WES is notable for increasing the ability to provide diagnostic capabilities in fetuses with sonographic abnormalities due to rare disorders. The identification of the abnormal gene will help to offer either preimplantation genetic diagnosis or prenatal invasive testing in these couples. VP33.09 Exome sequencing versus gene panels for non-immune hydrops fetalis