A Case of Aplasia Cutis Congenita Group 4
Journal of the Korean Society of Neonatology
;
: 77-80, 1998.
Article
Dans Coréen
| WPRIM
| ID: wpr-183909
ABSTRACT
Aplasia cutis congenita is a rare disorder characterized by localized or generalized absence of skin at birth. Group 4 in Friden's classification, which is associated with embryologic malformations including myelomeningocele, encephalomeningocele, omphalocele, gastroschisis. The authors have experienced a case of aplasia cutis congenita of right frontal scalp associated with bony defect, forming encephalocele in a newborn. We reported this case with brief review of literatures.
Texte intégral:
Disponible
Indice:
WPRIM (Pacifique occidental)
Sujet Principal:
Cuir chevelu
/
Peau
/
Dysplasie ectodermique
/
Myéloméningocèle
/
Classification
/
Laparoschisis
/
Parturition
/
Encéphalocèle
/
Hernie ombilicale
Limites du sujet:
Humains
/
Nouveau-né
langue:
Coréen
Texte intégral:
Journal of the Korean Society of Neonatology
Année:
1998
Type:
Article
Documents relatifs à ce sujet
MEDLINE
...
LILACS
LIS