
doi: 10.1542/peds.89.1.81
pmid: 1728027
A series of 1790 fetal and neonatal autopsies performed between 1976 and 1988 were retrospectively investigated for the presence of hydrops. Thirty (5.5%) and 35 (2.8%) cases of hydrops were found in the groups of fetal and neonatal autopsies, respectively. Genetic causes accounted for 35%. A careful search for previously reported genetic causes of fetal hydrops indicated 64 different etiologies. Twenty-one of them were not mentioned in the previous reviews: these include 9 skeletal dysplasias, 5 inborn errors of metabolism, 3 autosomal recessive, 3 autosomal dominant conditions, and 1 chromosomal abnormality
Chromosome Aberrations, Hydrops Fetalis, Infant, Newborn, Chromosome Disorders, Genes, Recessive, Bone and Bones, Humans, Metabolism, Inborn Errors, Genes, Dominant, Retrospective Studies
Chromosome Aberrations, Hydrops Fetalis, Infant, Newborn, Chromosome Disorders, Genes, Recessive, Bone and Bones, Humans, Metabolism, Inborn Errors, Genes, Dominant, Retrospective Studies
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