Aplasia cutis congenita: a case report
- PMID: 16409924
Aplasia cutis congenita: a case report
Abstract
Aplasia cutis congenita is a rare anomaly presenting with absence of skin. The most common site is the scalp. No definite etiology is available. Heredity is proposed with not much evidence. We present an instance with ACC occurring in both mother and son, suggesting a hereditary etiology.
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