Abstract
RASopathies are a large group of malformation syndromes caused by variants in genes encoding the Ras/mitogen-activated protein kinase signaling pathway. RASopathies are known to frequently cause nonimmune hydrops fetalis (NIHF). The contribution of parental inheritance of RASopathy causing NIHF is limited. Our objective was to review the genetic characteristics and prenatal phenotype of NIHF cases due to RASopathy.
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