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| | Rubella, congenital syndrome (Site not responding. Last check: 2007-10-09) |
 | | Cataracts/congenital glaucoma, congenital heart disease (most commonly patent ductus arteriosus, peripheral pulmonary artery stenosis), loss of hearing, pigmentary retinopathy B. Purpura, splenomegaly, jaundice, microcephaly, mental retardation, meningo-encephalitis, radiolucent bone disease. |
 | | Laboratory Criteria for Diagnosis: Isolation of rubella virus, OR Demonstration of rubella-specific IgM antibody, OR An infant's rubella antibody level that persists above and beyond the expected from passive transfer of maternal antibody (i.e., rubella titer that does not drop at the expected rate of a twofold dilution per month). |
 | | Reporting Procedure: All reports should be filed on Wyoming form WYEPI1.96 on the day of diagnosis followed by CDC form 71.17, Congenital Rubella Syndrome Case Report within seven days of diagnosis. |
| wdhfs.state.wy.us /dx_criteria/rubell2.htm (274 words) |
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