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Two Cases of Aplasia Cutis Congenita / 대한피부과학회지
Korean Journal of Dermatology ; : 83-87, 1985.
Article in Korean | WPRIM | ID: wpr-13848
ABSTRACT
Aplasia cutis congenita is an anomaly characterized by absence of localized areas of the integument. The most common type of aplasia cutis congenita is a circular or oval, sharply outlined ulcer 1 to 3cm in diameter on the vertex of the scalp at the level of the posterior fontanel. Two cases of aplasia cutis congenita are presented. The first case was in a male newborn infant with a localized defect on his scalp. The second case was also in a male newborn infant who had extensive symmetrical involvement of his heels. No similar conditions and associating other congenital anomalies were found in the family members of reported cases.
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Full text: Available Index: WPRIM (Western Pacific) Main subject: Scalp / Ulcer / Ectodermal Dysplasia / Heel / Cranial Fontanelles Limits: Humans / Male / Infant, Newborn Language: Korean Journal: Korean Journal of Dermatology Year: 1985 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Scalp / Ulcer / Ectodermal Dysplasia / Heel / Cranial Fontanelles Limits: Humans / Male / Infant, Newborn Language: Korean Journal: Korean Journal of Dermatology Year: 1985 Type: Article