A Case of Congenital Rubella Syndrome
Journal of the Korean Society of Neonatology
;
: 104-108, 1998.
Article
in Korean
| WPRIM
| ID: wpr-126179
ABSTRACT
We experienced a case of congenital rubella syndrome manifesting patent ductus arteriosus, petechiae, microcephaly, intrauterine growth retardation, and hepatomegaly in one-day-old female newborn infant. Congenital rubella syndrome was confirmed by positive results of anti-rubella IgM in the sera of patient. Anti-rubella IgM was negative in the sera of mother, while anti-rubella IgG was positive.
Full text:
Available
Index:
WPRIM (Western Pacific)
Main subject:
Purpura
/
Rubella Syndrome, Congenital
/
Immunoglobulin G
/
Immunoglobulin M
/
Ductus Arteriosus, Patent
/
Fetal Growth Retardation
/
Hepatomegaly
/
Microcephaly
/
Mothers
Limits:
Female
/
Humans
/
Infant, Newborn
Language:
Korean
Journal:
Journal of the Korean Society of Neonatology
Year:
1998
Type:
Article
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