Your browser doesn't support javascript.
loading
A Case of Congenital Rubella Syndrome
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.
Subject(s)
Key words
Full text: 1 Index: WPRIM Main subject: Purpura / Rubella Syndrome, Congenital / Immunoglobulin G / Immunoglobulin M / Ductus Arteriosus, Patent / Fetal Growth Retardation / Hepatomegaly / Microcephaly / Mothers Limits: Female / Humans / Newborn Language: Ko Journal: Journal of the Korean Society of Neonatology Year: 1998 Type: Article
Full text: 1 Index: WPRIM Main subject: Purpura / Rubella Syndrome, Congenital / Immunoglobulin G / Immunoglobulin M / Ductus Arteriosus, Patent / Fetal Growth Retardation / Hepatomegaly / Microcephaly / Mothers Limits: Female / Humans / Newborn Language: Ko Journal: Journal of the Korean Society of Neonatology Year: 1998 Type: Article