A Case of Congenital Rubella Syndrome
Journal of the Korean Society of Neonatology
;
: 104-108, 1998.
Artículo
en Coreano
| 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.
Texto completo:
Disponible
Índice:
WPRIM (Pacífico Occidental)
Asunto principal:
Púrpura
/
Síndrome de Rubéola Congénita
/
Inmunoglobulina G
/
Inmunoglobulina M
/
Conducto Arterioso Permeable
/
Retardo del Crecimiento Fetal
/
Hepatomegalia
/
Microcefalia
/
Madres
Límite:
Femenino
/
Humanos
/
Recién Nacido
Idioma:
Coreano
Revista:
Journal of the Korean Society of Neonatology
Año:
1998
Tipo del documento:
Artículo
Similares
MEDLINE
...
LILACS
LIS