Prevention of Congenital Rubella Infection: Symposium Summary

1985 ◽  
Vol 7 (Supplement_1) ◽  
pp. S212-S215 ◽  
Author(s):  
Alan R. Hinman
1989 ◽  
Vol 64 (9) ◽  
pp. 1280-1283 ◽  
Author(s):  
N J Wild ◽  
S Sheppard ◽  
R W Smithells ◽  
H Holzel ◽  
G Jones

2014 ◽  
Vol 60 (5) ◽  
pp. 451-456
Author(s):  
Suely Pires Curti ◽  
Cristina Adelaide Figueiredo ◽  
Maria Isabel de Oliveira ◽  
Joelma Queiroz Andrade ◽  
Marcelo Zugaib ◽  
...  

Objective: rubella during the early stages of pregnancy can lead to severe birth defects known as congenital rubella syndrome (CRS). Samples collected from pregnant women with symptoms and suspected of congenital rubella infection between 1996 and 2008 were analyzed. Methods: a total of 23 amniotic fluid samples, 16 fetal blood samples, 1 product of conception and 1 placenta were analyzed by serology and RT-PCR. Results: all patients presented positive serology for IgG / IgM antibodies to rubella virus. Among neonates, 16 were IgG-positive, 9 were IgM-positive and 4 were negative for both antibodies. Of the 25 samples analyzed in this study, 24 were positive by RT-PCR. Changes in ultrasound were found in 15 (60%) of 25 fetuses infected with rubella virus. Fetal death and miscarriage were reported in 10 (40%) of the 25 cases analyzed. The rubella virus was amplified by PCR in all fetuses with abnormal ultrasound compatible with rubella. Fetal death and abortion were reported in 10 of 25 cases analyzed. Conclusion: this study, based on primary maternal rubella infection definitely confirms the good sensitivity and specificity of RT-PCR using amniotic fluid and ultrasound. The results showed that molecular assays are important tools in the early diagnosis of rubella and congenital rubella syndrome.


PEDIATRICS ◽  
2001 ◽  
Vol 108 (6) ◽  
pp. 1389-1390 ◽  
Author(s):  
D. M. Zerr ◽  
J. Heath ◽  
D. Riggert ◽  
E. K. Marcuse ◽  
L. Zimmerman ◽  
...  

Author(s):  
Anthony R. Mawson ◽  
Ashley M. Croft

Rubella is a systemic virus infection that is usually mild. It can, however, cause severe birth defects known as the congenital rubella syndrome (CRS) when infection occurs early in pregnancy. As many as 8%–13% of children with CRS developed autism during the rubella epidemic of the 1960s compared to the background rate of about 1 new case per 5000 children. Rubella infection and CRS are now rare in the U.S. and in Europe due to widespread vaccination. However, autism rates have risen dramatically in recent decades to about 3% of children today, with many cases appearing after a period of normal development (‘regressive autism’). Evidence is reviewed here suggesting that the signs and symptoms of rubella may be due to alterations in the hepatic metabolism of vitamin A (retinoids), precipitated by the acute phase of the infection. The infection causes mild liver dysfunction and the spillage of stored vitamin A compounds into the circulation, resulting in an endogenous form of hypervitaminosis A. Given that vitamin A is a known teratogen, it is suggested that rubella infection occurring in the early weeks of pregnancy causes CRS through maternal liver dysfunction and exposure of the developing fetus to excessive vitamin A. On this view, the multiple manifestations of CRS and associated autism represent endogenous forms of hypervitaminosis A. It is further proposed that regressive autism results primarily from post-natal influences of a liver-damaging nature and exposure to excess vitamin A, inducing CRS-like features as a function of vitamin A toxicity, but without the associated dysmorphogenesis. A number of environmental factors are discussed that may plausibly be candidates for this role, and suggestions are offered for testing the model. The model also suggests a number of measures that may be effective both in reducing the risk of fetal CRS in women who acquire rubella in their first trimester and in reversing or minimizing regressive autism among children in whom the diagnosis is suspected or confirmed.


1991 ◽  
Vol 107 (1) ◽  
pp. 63-68 ◽  
Author(s):  
C. L. Miller

Before Gregg's historic observation [1] rubella was not considered to have clinical or epidemiological importance in any country. In the western world epidemics occurred at varying intervals but with little morbidity and apparently only minor complications. Despite confirmation of Gregg's findings from many quarters, it was not until the worldwide outbreaks in the 1960s that the aftermath of rubella infection in pregnancy was fully realized. As a result of the 1964 outbreak in New York City, more than 1000 children were born with congenital rubella syndrome (CRS) and over 300 pregnancies either aborted spontaneously or were terminated for rubella infection [2]. The number of children affected represented 1% of births in the city; if extrapolated to the whole country this gave an estimated total of 30000 cases of CRS. No such disasters have so far been reported from the developing world.


1985 ◽  
Vol 7 (Supplement_1) ◽  
pp. S56-S63 ◽  
Author(s):  
Reisaku Kono ◽  
Munehiro Hirayama ◽  
Chieko Sugishita ◽  
Kikuko Miyamura

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