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Congenital rubella syndrome CDC case definitions

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Kalsang Dolma, M.B.B.S.[2], Dima Nimri, M.D. [3]

Overview

In 2009, the CDC published the case classification of congenital rubella syndrome and divided into suspected cases, probable cases, confirmed cases and infection only, based on symptoms and/or laboratory findings.[1]

CDC Case Definitions

in 2009, the CDC published the following case definition for case classification of congenital rubella syndrome:[1]

Case Classification Criteria
Suspected An infant who does not meet the criteria for a probable or confirmed case but who has one or more of the following findings:
Probable An infant who does not have laboratory confirmation of rubella infection but has at least two of the following, without a more plausible etiology:

OR

An infant who does not have laboratory confirmation of rubella infection but has at least one or more of the following, without a more plausible etiology:

AND

One or more of the following:

Confirmed An infant with at least one of the symptoms clinically consistent with congenital rubella syndrome listed above; and laboratory evidence of congenital rubella infection demonstrated by:
  1. Isolation of rubella virus, OR
  2. Detection of rubella-specific immunoglobulin M (IgM) antibody, OR
  3. Infant rubella antibody level that persists at a higher level and for a longer period of time than expected from passive transfer of maternal antibody (i.e., rubella titer that does not drop at the expected rate of a two-fold decline per month), OR
  4. A specimen that is PCR-positive for rubella virus
Infection only An infant without any clinical symptoms or signs of rubella but with laboratory evidence of infection demonstrated by:

References

  1. 1.0 1.1 Center for Disease Control and Prevention https://www.cdc.gov/vaccines/pubs/surv-manual/chpt15-crs.html. Accessed on Jan 5, 2017

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