✦ LIBER ✦

Prenatal diagnosis of congenital anomalies in an intrauterine growth retarded fetus

✍ Scribed by Mitchell S. Golbus; Bryan D. Hall; Robert K. Creasy

Publisher: Springer
Year: 1976
Tongue: English
Weight: 341 KB
Volume: 32
Category: Article
ISSN: 0340-6717
DOI: 10.1007/bf00295828

No coin nor oath required. For personal study only.

✦ Synopsis

Chromosome analysis of amniotic fluid cells and amniotic fluid alpha-fetoprotein determinations were used to investigate a fetus with severe intrauterine growth retardation in the third trimester. The karyotype was 47,XY,18+ and increased alpha-fetoprotein levels indicated the presence of congenital malformations. We suggest that when severe fetal growth retardation is detected early in the antepartum course, amniotic fluid alpha-fetoprotein and amniotic fluid cell chromosome studies be done to determine if congenital anomalies may be an etiological factor.

📜 SIMILAR VOLUMES

Prenatal sonographic diagnosis of congen

Prenatal sonographic diagnosis of congenital heart disease and intrauterine growth restriction: A case–control study

✍ Annette Perez-Delboy; Lynn L. Simpson 📂 Article 📅 2007 🏛 John Wiley and Sons 🌐 English ⚖ 107 KB

## 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

Lambotte syndrome: Microcephaly, holopro

Lambotte syndrome: Microcephaly, holoprosencephaly, intrauterine growth retardation, facial anomalies, and early lethality—A new sublethal multiple congenital anomaly/mental retardation syndrome in four sibs

✍ Verloes, A. ;Dodinval, P. ;Beco, L. ;Bonnivert, J. ;Lambotte, C. 📂 Article 📅 1990 🏛 John Wiley and Sons 🌐 English ⚖ 532 KB

Sonographic diagnosis of intrauterine gr

Sonographic diagnosis of intrauterine growth retardation in a dichorionic diamniotic twin

✍ Howard Weinstein; Beverly A. Spirt 📂 Article 📅 1979 🏛 John Wiley and Sons 🌐 English ⚖ 216 KB

Three-level view of fetal brain imaging

Three-level view of fetal brain imaging in the prenatal diagnosis of congenital anomalies

✍ E. Albert Reece; Israel Goldstein 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 337 KB 👁 2 views

Objective: To determine whether a systematic stream-lined approach could be routinely used in the evaluation of fetal intracranial anatomy. Methods: Nine thousand six hundred uncomplicated pregnancies were evaluated using a three-level view of fetal brain imaging. An axial scan, which passed through

Prenatal growth retardation, microcephal

Prenatal growth retardation, microcephaly, and eye coloboma in infant with multiple congenital anomalies: Further delineation of presumed new dysmorphic syndrome

✍ Goran Cuturilo; Ida Jovanovic; Goran Vukomanovic; Milan Djukic; Igor Stefanovic; 📂 Article 📅 2008 🏛 John Wiley and Sons 🌐 English ⚖ 249 KB 👁 1 views

## Abstract ## BACKGROUND: Ten years ago an unusual association of prenatal growth retardation, microcephaly, coloboma of the iris/eye anomalies, congenital heart defects, and urogenital anomalies was reported for the first time in three siblings. Autosomal recessive inheritance was presumed. This

Prenatal diagnosis of congenital varicel

Prenatal diagnosis of congenital varicella syndrome and detection of varicella-zoster virus in the fetus: a case report

✍ John Hartung; Gisela Enders; Rabih Chaoui; Annette Arents; Cornelia Tennstedt; R 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 220 KB 👁 3 views

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