http://www.cdc.gov/epo/dphsi/casedef/rubella_syndrome_congenital_current.htm
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Rubella Syndrome, Congenital - 1999 Case Definition
Revised May 1999
Clinical descriptionPresence of any defect(s) or laboratory data consistent with congenital rubella infection. Infants with congenital rubella syndrome usually present with more than one sign or symptom consistent with congenital rubella infection. However, infants may present with a single defect. Deafness is most common single defect. Laboratory criteria for diagnosis
Clinical case definitionAn illness, usually manifesting in infancy, resulting from rubella infection in utero and characterized by signs or symptoms from the following categories:
Case classificationSuspected: A case with some compatible clinical findings but not meeting the criteria for a probable case. Probable: A case that is not laboratory confirmed and that has any two complications listed in paragraph "a" of the clinical case definition or one complication from paragraph "a" and one from paragraph "b", and lacks evidence of any other etiology. Confirmed: A clinically consistent case that is laboratory confirmed. Infection only: A case that demonstrates laboratory evidence of infection, but without any clinical symptoms or signs. NoteIn probable cases, either or both of the eye-related findings (cataracts and congenital glaucoma) count as a single complication. In cases classified as infection only, if any compatible signs or symptoms (e.g., hearing loss) are identified later, the case is reclassified as confirmed. See also: |
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