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Fetal hydrops Boyd PA; Keeling JWJ Med Genet 1992[Feb]; 29 (2): 91-7Seventy-two fetuses or neonates with non-immune hydrops were examined between 1983 and 1988. The commonest association was chromosome abnormality; 11 fetuses had a 45,X karyotype and 11 autosomal trisomy. Chromosome abnormality was suspected in a further 20 on necropsy findings but chromosome culture was not possible or unsuccessful. In 11 cases there was histological evidence of infection; seven babies had major structural anomalies and six affected fetuses were twins. In six (8%) the cause of hydrops was not determined compared with eight (16%) of cases examined between 1976 and 1982. Hydrops was diagnosed more frequently while the fetus was alive, before 20 weeks' gestation, and associated with chromosome anomaly than found previously.|Chromosome Aberrations[MESH]|Diseases in Twins[MESH]|Female[MESH]|Gestational Age[MESH]|Humans[MESH]|Hydrops Fetalis/*diagnosis/etiology/genetics[MESH]|Infections/complications[MESH]|Pregnancy[MESH]|Prenatal Diagnosis[MESH]|Viscera/abnormalities[MESH] |
