Fourteen fetuses at risk of Varicella-Zoster virus (VZV) infection underwent prenatal diagnosis at 10-24 weeks' gestation by a combination of chorionic villus sampling, amniocentesis, and fetal blood sampling. Polymerase chain reaction (PCR) was done on fetal and placental tissues, using primers whi
PRENATAL SONOGRAPHIC DIAGNOSIS OF CONGENITAL VARICELLA INFECTION—A CASE REPORT
✍ Scribed by G. J. HOFMEYR; S. MOOLLA; T. LAWRIE
- Publisher
- John Wiley and Sons
- Year
- 1996
- Tongue
- English
- Weight
- 882 KB
- Volume
- 16
- Category
- Article
- ISSN
- 0197-3851
No coin nor oath required. For personal study only.
✦ Synopsis
We report a case of fetal varicella infection following the diagnosis of maternal varicella infection at 13 weeks of pregnancy. Anomalies noted sonographically at 26 weeks' gestation included oligohydramnios, symmetrically impaired fetal growth, limb anomalies, a thin placenta, and widespread dystrophic calcification of the abdominal cavity and chest, including the lungs and myocardium. Some of these sonographic anomalies have been reported previously. However, to our knowledge, prenatal diagnosis of calcification of the lungs and myocardium has not been described.
📜 SIMILAR VOLUMES
Varicella syndrome (VS) specific malformations were sonographically seen at 22 weeks and 3 days of gestation. Fetal infection was demonstrated by detection of varicella-zoster virus (VZV) DNA in fetal blood and amniotic fluid by polymerase chain reaction (PCR). Following therapeutic abortion, fetal
## Abstract We describe the abnormal sonographic findings in the brain of a 26‐week fetus, which increased the suspicion of isolated lissencephaly. Follow‐up ultrasound examination and MRI depicted diffuse cortical agyria, microcephaly, hypotelorism, and proptosis. Cordocentesis showed a normal 46,
## Abstract ## Purpose To determine the prevalence of intrauterine growth restriction (IUGR) in cases of congenital heart disease (CHD) and to evaluate whether the prenatal diagnosis of isolated CHD was a significant risk factor for IUGR. ## Methods We conducted a retrospective case–control stud
Primary benign intracardiac tumours in the infant period are rare. We report a case of a cardiac osteoma detected at 17 weeks of gestation. Ultrasonographically, it appeared as a calcified mass with a sharp margin and was associated with hypoplastic right ventricle. The gross and histological findin