A Case of Congenital Rubella Syndrome
Journal of the Korean Society of Neonatology
; : 104-108, 1998.
Article
in Ko
| WPRIM
| ID: wpr-126179
Responsible library:
WPRO
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.
Key words
Full text:
1
Index:
WPRIM
Main subject:
Purpura
/
Rubella Syndrome, Congenital
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Immunoglobulin G
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Immunoglobulin M
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Ductus Arteriosus, Patent
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Fetal Growth Retardation
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Hepatomegaly
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Microcephaly
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Mothers
Limits:
Female
/
Humans
/
Newborn
Language:
Ko
Journal:
Journal of the Korean Society of Neonatology
Year:
1998
Type:
Article