1.
Journal of the Korean Society of Neonatology
;
: 77-80, 1998.
Article
in Korean
| 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.