FETAL CYSTIC HYGROMA - PRENATAL-DIAGNOSIS AND MANAGEMENT
- 1 August 1988
- journal article
- research article
- Vol. 72 (2) , 223-224
Abstract
Seventeen cases of fetal cystic hygroma detected during ultrasound examination are reported. In nine instances, associated abnormalities were recognized, such as fetal hydrops and a two-vessel cord. All diagnoses were confirmed at autopsy. Karyotyping revealed normal findings in six cases, Turner''s syndrome in eight cases, and Edwards'' syndrome in one case; culture failure occurred in the remaining two cases. An ultrasound diagnosis of cystic hygroma should be followed by a careful search for other anomalies and by fetal karyotyping. Afterward, genetic counseling is indicated.This publication has 3 references indexed in Scilit:
- Nuchal cysts syndromes: Etiology, pathogenesis, and prenatal diagnosisAmerican Journal of Medical Genetics, 1985
- Cystic hygroma: Prenatal diagnosis and genetic counsellingPrenatal Diagnosis, 1985
- Fetal Cystic HygromaNew England Journal of Medicine, 1983