Purpose. We evaluated the reliability of prenatal sonography and the usefulness of the umbilical vein and artery diameter ratio, transverse umbilical artery diameter, and systolic-diastolic ratio in detecting single umbilical artery (SUA). Methods. In 24 of 6,970 fetuses, SUA was detected using pre
PRENATAL DIAGNOSIS AND CLINICAL SIGNIFICANCE OF HYPOPLASTIC UMBILICAL ARTERY
โ Scribed by BORIS PETRIKOVSKY; ELIZABETH SCHNEIDER
- Publisher
- John Wiley and Sons
- Year
- 1996
- Tongue
- English
- Weight
- 386 KB
- Volume
- 16
- Category
- Article
- ISSN
- 0197-3851
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โฆ Synopsis
This study reports the maternal, fetal, and neonatal outcomes in cases with hypoplastic umbilical artery. The sonographic finding of a three-vessel umbilical cord showing an artery-to-artery diameter difference of more than 50 per cent was defined as hypoplastic umbilical artery. All fetuses diagnosed with hypoplastic umbilical artery underwent genetic amniocentesis and ultrasound. Fetal, maternal, and neonatal outcomes were analysed. Twelve fetuses with hypoplastic umbilical artery were detected over a 6-year period (1989)(1990)(1991)(1992)(1993)(1994)(1995). Associated abnormalities included trisomy 18 (one case), polyhydramnios (three cases), congenital heart disease (one case), and fetal growth restriction (two cases). Maternal diabetes was detected in four cases. The pregnancy was terminated in one case; one neonate with severe fetal growth restriction expired; and one survived with congenital heart disease. The presence of hypoplastic umbilical artery was associated with increased perinatal morbidity and congenital abnormalities. Diabetes was frequently detected. Fetal surveillance and echocardiography are indicated in cases of hypoplastic umbilical artery.
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Prior to the age of invasive fetal procedures, spontaneous hematomas of the umbilical cord were extremely rare events. Seventeen of the 36 cases (47%) of umbilical cord hematomas reported in the world literature resulted in fetal demise.' Postpartum examination of the cord and placenta in these case
The association of rare chromosomal rearrangements involving a specific 10q breakpoint with a single umbilical artery (SUA) and sex reversal has never been reported. This report describes the case of a fetus with prenatal ultrasound features of severe intrauterine growth retardation (IUGR), congenit