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Medical Definition of Aplasia cutis congenita
1. Congenital absence or deficiency of a localised area of skin, with the base of the defect covered by a thin translucent membrane; most often a single area near the vertex of the scalp, but may occur in other areas; underlying structures may also be affected; autosomal inheritance, either dominant or recessive. (05 Mar 2000)
Lexicographical Neighbors of Aplasia Cutis Congenita
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