Congenital rubella syndrome: Difference between revisions
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Revision as of 19:45, 9 December 2011
For patient information, click here
Congenital rubella syndrome | |
Cataracts due to congenital rubella syndrome | |
ICD-10 | P35.0 |
ICD-9 | 771.0 |
DiseasesDB | 11729 |
MedlinePlus | 001658 |
MeSH | D012410 |
Overview
Congenital rubella syndrome (CRS) can occur in a developing fetus of a pregnant woman who has contracted rubella during her first trimester. Problems rarely occur when rubella is contracted by the mother after 20 weeks of gestation. In 1941 it was discovered by Australian Norman McAllister Gregg (1892-1966).
Complications
CRS can result in serious birth defects such as:
- malformations of the heart (especially patent ductus arteriosus), eyes or brain
- deafness
- spleen, liver or bone marrow problems (some of which may disappear shortly after birth)
- mental retardation
- small head size (microcephaly)
- eye defects
- low birth weight
- thrombocytopenic purpura
- hepatomegaly
Treatment
Children who have been exposed to rubella in the womb should also be watched closely as they age for any indication of the following:
Template:Certain conditions originating in the perinatal period de:Rötelnembryofetopathie fi:Synnynnäinen vihurirokko-oireyhtymä