A Case of Aplasia Cutis Congenita Group 5
Journal of the Korean Society of Neonatology
;
: 272-275, 1997.
Artículo
en Coreano
| WPRIM
| ID: wpr-121129
ABSTRACT
Aplasia cutis congenita is a rare disorder characterized by localized or generalized absence of skin at birth. The various hypothesis and classification are proposed. Type V in Frieden's classification, which is associated with fetus papyraceus or placental infarcts, occurs as a large cutaneous defect on the trunk and extremities. We experienced the patient had skin defect affecting the lower abdomen symmetrically, with no family history of the any disorders or chromosomal anomalies and associated anomalies. A twin fetus was died in utero. We report a case of aplasia cutis congenita associated with fetus papyraceus with the review of the associated literatures.
Texto completo:
Disponible
Índice:
WPRIM (Pacífico Occidental)
Asunto principal:
Piel
/
Gemelos
/
Displasia Ectodérmica
/
Clasificación
/
Parto
/
Abdomen
/
Extremidades
/
Feto
Límite:
Humanos
Idioma:
Coreano
Revista:
Journal of the Korean Society of Neonatology
Año:
1997
Tipo del documento:
Artículo
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