A Case of 4q Deletion with Partial Agenesis of Corpus Callosum
Journal of the Korean Pediatric Society
;
: 273-277, 2002.
Artículo
en Coreano
| WPRIM
| ID: wpr-13329
ABSTRACT
Syndrome of 4q deletion is characterized by an abnormal shape of the skull, craniofacial dysmorphism, cardiovascular malformations, genitourinary defects, limb and digital anomalies, and developmental delay. We experienced a case of 4q interstitial deletion in a 2 day-old female neonate who showed short extremities, partial agenesis of corpus callosum and congenital heart defects. We report the case with a brief review of the literature.
Texto completo:
Disponible
Índice:
WPRIM (Pacífico Occidental)
Asunto principal:
Cráneo
/
Cromosomas Humanos Par 4
/
Extremidades
/
Agenesia del Cuerpo Calloso
/
Cardiopatías Congénitas
Límite:
Femenino
/
Humanos
/
Recién Nacido
Idioma:
Coreano
Revista:
Journal of the Korean Pediatric Society
Año:
2002
Tipo del documento:
Artículo
Similares
MEDLINE
...
LILACS
LIS