Aplasia cutis congenita (Q46678): Difference between revisions
From determinar.ia.br - Determine suas informações
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Changed label, description and/or aliases in pt-br, en |
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| description / pt-br | description / pt-br | ||
Ausência congênita de pele. A forma mais comum apresenta-se como uma anomalia limitada ao couro cabeludo. É também um componente de várias síndromes genéticas. | |||
| description / en | description / en | ||
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. | |||
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. |
