scholarly journals Prenatal diagnosis of single umbilical artery complicated by intrauterine growth retardation and preterm labor: Case report

2019 ◽  
Vol 8 (6) ◽  
pp. 2151
Author(s):  
IbrahimA Abdelazim ◽  
Mohannad Abu-Faza ◽  
MohamedE. S. Hamed ◽  
OsamaO Amer ◽  
Svetlana Shikanova ◽  
...  
2016 ◽  
Vol 1 (1) ◽  

The Umbilical Artery Unica is found in 0.2 to 1.1% of all fetuses. Their presence of AOU in itself does not cause any harm to the fetus and newborn. Sometimes, however, this abnormality occurs associated with chromosomal abnormalities and other abnormalities Structural. The chromosomal abnormalities account for about 5-10%; the most common are trisomy 13, 18 and 21. The non-chromosomal anomalies associated together account for about 22%: heart disease is the most frequent. 4-6% of fetuses with AOU in isolation have minor abnormalities at birth, whose ultrasound diagnosis is difficult or impossible. 25-30% of fetuses with AOU are suffering from intrauterine growth retardation (IUGR), and about a quarter of these born prematurely. Fetuses with AOU also feature a higher risk of death intrauterine and / or intrapartum.


2016 ◽  
Vol 1 (1) ◽  

The Umbilical Artery Unica is found in 0.2 to 1.1% of all fetuses. Their presence of AOU in itself does not cause any harm to the fetus and newborn. Sometimes, however, this abnormality occurs associated with chromosomal abnormalities and other abnormalities Structural. The chromosomal abnormalities account for about 5-10%; the most common are trisomy 13, 18 and 21. The non-chromosomal anomalies associated together account for about 22%: heart disease is the most frequent. 4-6% of fetuses with AOU in isolation have minor abnormalities at birth, whose ultrasound diagnosis is difficult or impossible. 25-30% of fetuses with AOU are suffering from intrauterine growth retardation (IUGR), and about a quarter of these born prematurely. Fetuses with AOU also feature a higher risk of death intrauterine and / or intrapartum.


1985 ◽  
Vol 2 (01) ◽  
pp. 49-54 ◽  
Author(s):  
Usha Chitkara ◽  
Gertrud Berkowitz ◽  
Rebecca Levine ◽  
David Riden ◽  
Richard Fagerstrom, Jr. ◽  
...  

BMJ ◽  
1990 ◽  
Vol 300 (6731) ◽  
pp. 1044-1045 ◽  
Author(s):  
G Burke ◽  
B Stuart ◽  
P Crowley ◽  
S N Scanaill ◽  
J Drumm

2015 ◽  
Vol 18 (5) ◽  
pp. 601-605 ◽  
Author(s):  
Lucia Pasquini ◽  
Silvia Conticini ◽  
Tiziana Tomaiuolo ◽  
Giovanni Sisti ◽  
Viola Seravalli ◽  
...  

We report our experience on the application of Gratacos’ classification in a cohort of monochorionic pregnancies complicated by selective intra-uterine growth retardation based on the Doppler assessment of the umbilical artery. Materials and methods: A retrospective study was conducted on 52 cases of monochorionic twin pregnancies, in which one twin presented an abdominal circumference at or below the 10th percentile for gestational age. Cases were classified into three types according to the umbilical artery Doppler in the smaller twin. Subsequently, patients were divided into two groups: the selective IntraUterine Growth Retardation group and the Twin-to-Twin Transfusion Syndrome (TTTS) group. Results: Of the total 52 cases, 37 were classified as Type I, 12 as Type II, and 3 as Type III cases. In the total group, progressive fetal deterioration of the smaller fetus requiring active management was observed in 66.7% of Type II and 11.1% of Type I cases (p < .001), and in no Type III case. Unexpected fetal death of the smaller twin was observed more frequently in Type III (two cases, 66.7%) than in Types I and II cases (5% and 33%, respectively). Among the 52 cases, TTTS with oligo-polyhydramnios sequence was diagnosed in 10 cases. The remaining 42 cases were therefore defined as selective intra-uterine growth retardation. In the selective IntraUterine Growth Retardation group, results were similar to those obtained for the whole population. Conclusions: Classification of complicated monochorionic twins based on the umbilical artery Doppler is particularly important for counseling, even when we include TTTS cases, and permits the prediction of clinical evolution and perinatal outcome.


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