Congenital rubella syndrome laboratory findings
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Dima Nimri, M.D. [2]
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Overview
Laboratory Findings
Prenatal Testing
Ultrasound
Not all fetuses infected with rubella virus in the prenatal period show visible signs on ultrasound consistent with congenital rubella syndrome. However, positive findings on ultrasound provide certainty to the diagnosis. Such findings include:[1]
- Fetal hydrops
- Bowel hyperechogenicity
- Intrauterine growth retardation (IUGR)
Invasive Techniques
Several invasive techniques can be done during pregnancy, depending on the gestational age. These techniques include:[1][2]
Technique | Timing/ Gestational age at which it is performed | Results | Complications |
---|---|---|---|
Amniocentesis | after 15 weeks |
|
|
Fetal blood sampling | after 18-20 weeks | ||
Chorionic villus sampling | after 11 weeks |
Post-natal Serologic Testing
References
- ↑ 1.0 1.1 De Santis M, Cavaliere AF, Straface G, Caruso A (2006). "Rubella infection in pregnancy". Reprod. Toxicol. 21 (4): 390–8. doi:10.1016/j.reprotox.2005.01.014. PMID 16580940.
- ↑ Morgan-Capner P, Hodgson J, Hambling MH, Dulake C, Coleman TJ, Boswell PA, Watkins RP, Booth J, Stern H, Best JM (1985). "Detection of rubella-specific IgM in subclinical rubella reinfection in pregnancy". Lancet. 1 (8423): 244–6. PMID 2857319.