Congenital rubella syndrome

Congenital rubella syndrome (CRS) is an infectious embryofetopathy that may present in an infant as a result of maternal infection and subsequent fetal infection with rubella virus. CRS can lead to deafness, cataract, and variety of other permanent manifestations including cardiac and neurological defects.

Erythema

Redness of the skin, caused by hyperemia of the capillaries in the lower layers of the skin.


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PMID (PMCID)
8051318
 MALE Infant
Congenital rubella syndrome with rubella virus-associated generalized brownish macules, indurated erythemas, papules, and pigmentation.
Seno A, Tada J, Matsuura H, Arata J, Isomura H, Kitamura T, Oda M, Katow S.
J Dermatol. 1994;21(5):323-8.
Congenital rubella syndrome with rubella virus-associated generalized brownish macules, indurated erythemas, papules, and pigmentation.