The objective of our study was to appraise the incidence and significance of persistent right umbilical vein (PRUV), the most common foetal venous aberration. Based on a south Indian antenatal cohort, we identified 23 cases of PRUV amongst 20,452 foetuses of consecutive pregnancies, from 2009 to 2014, yielding an incidence of 1 in 889 total births (0.11%). The median maternal age was 24 (IQR, 22-26) years, and median gestational age at diagnosis was 23 (IQR, 22-24) weeks. Intrahepatic drainage of PRUV was seen in 91.3% cases. In three cases (13%), ductus venosus was absent. In 52.2% of the cases, additional major abnormalities were observed - predominantly cardiovascular (39.1%). The common minor marker was single umbilical artery (13%). The karyotype was found to be normal in six cases (26%) which underwent invasive testing. When associated anomalies were inconsequential or absent, the postnatal outcome was good, which reflected in 60.9% of our cases.
We report a case of a rare balanced Robertsonian translocation, t (21q; 21q) in one of the parents that results in adverse pregnancy outcome in 100 % of cases, either first trimester miscarriages or Down syndrome in all viable fetuses. The case highlights the role of optimum genetic evaluation of all cases of reproductive disorders as they can have profound effect over prognosis and further management.
The chief objectives of our study were to assess the incidence and significance of fetal aberrant right subclavian artery (ARSA) in a nonreferral cohort of south Indian antenatal woman, and to compare it with other second trimester markers of Down syndrome. This was a prospective study conducted at Edappal hospital, India. After satisfying inclusion and exclusion criteria, 2000 consecutive antenatal women, seeking prenatal care and planning delivery at the same center, were recruited in a consecutive fashion. ARSA was identified as a retrotracheal arterial vessel in the axial three vessel trachea view, coursing towards right axilla. During February 2015 to January 2016, nine cases of ARSA were identified amongst 2000 antenatal women, yielding an incidence of 0.45 % (95 % CI 0.2-0.9 %). Of these, eight cases (8/9, 89 %) were isolated with normal karyotype, and negative for 22q11 microdeletion. Down syndrome was prenatally diagnosed in four cases (4/2000, 0.2 %), with ARSA detected in one case [sensitivity-25 %, specificity-99.6 %, positive likelihood ratio (?LR)-62.5 %, negative likelihood ratio (-LR)-0.75 %; Odds ratio 82.8 %, 95 % CI 7.8-883]. Of the significant second trimester minor markers, an absent nasal bone was the most common (13/ 2000, 0.65 %), followed by ARSA. All the isolated cases had normal neonatal outcomes. ARSA is relatively common second trimester aneuploidy marker, associated with high global ?LR but nil isolated ?LR. Indication for fetal karyotype in isolated cases seems to be weak.
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