A case of Roberts syndrome
Journal of the Korean Pediatric Society
;
: 1447-1451, 1993.
Artículo
en Coreano
| WPRIM
| ID: wpr-51318
ABSTRACT
Roberts syndrome is an autosomal recessive disorder accompanied by limb defects, craniofacial abnormalities, pre-and postnatal growth retardation. Patients with Roberts syndrome have characteristic premature separation of heterochromatin of many chromosomes and abnormalties in celldivision cycle. We have experienced a case of Roberts syndrome in an immature neonate The patients showed characteristic clinical features of multiple, severe facial mid-line clefts, and tetraphoco-amelia. The brief review of the literlature was made.
Texto completo:
Disponible
Índice:
WPRIM (Pacífico Occidental)
Asunto principal:
Heterocromatina
/
Anomalías Craneofaciales
/
Ectromelia
/
Extremidades
Límite:
Humanos
/
Recién Nacido
Idioma:
Coreano
Revista:
Journal of the Korean Pediatric Society
Año:
1993
Tipo del documento:
Artículo
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