Aplasia cutis congenita (Q46678): Difference between revisions
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Revision as of 15:26, 13 August 2026
Congenital absence of skin. The commonest form presents as a defect limited to the scalp. It is also a component of a number of genetic syndromes.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | LC60 |
||
| English | Aplasia cutis congenita |
Congenital absence of skin. The commonest form presents as a defect limited to the scalp. It is also a component of a number of genetic syndromes. |
