Temporal triangular alopecia (Q86220): Difference between revisions
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| description / pt-br | description / pt-br | ||
Alopecia triangular temporal é uma alopecia permanente circunscrita, não cicatricial e não inflamatória de causa desconhecida, confinada ao couro cabeludo frontotemporal. A área da perda de cabelo é comumente triangular, mas pode ser oval ou em forma de lanceta. Geralmente é unilateral. A alopecia está aparente desde o nascimento em cerca de um terço dos casos, mas pode não ser notada até a infância. Raramente tem sido associada à facomatose pigmentovascular. | |||
| description / en | description / en | ||
Temporal triangular alopecia is a circumscribed, non-scarring, non-inflammatory permanent alopecia of unknown cause confined to the frontotemporal scalp. The area of hair loss is commonly triangular but may be oval or lancet-shaped. It is usually unilateral. The alopecia is apparent from birth in about a third of cases but may not be noted until later childhood. It has, rarely, been associated with phakomatosis pigmentovascularis. | |||
Revision as of 11:35, 15 August 2026
Temporal triangular alopecia is a circumscribed, non-scarring, non-inflammatory permanent alopecia of unknown cause confined to the frontotemporal scalp. The area of hair loss is commonly triangular but may be oval or lancet-shaped. It is usually unilateral. The alopecia is apparent from birth in about a third of cases but may not be noted until later childhood. It has, rarely, been associated with phakomatosis pigmentovascularis.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_638542711 |
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| English | Temporal triangular alopecia |
Temporal triangular alopecia is a circumscribed, non-scarring, non-inflammatory permanent alopecia of unknown cause confined to the frontotemporal scalp. The area of hair loss is commonly triangular but may be oval or lancet-shaped. It is usually unilateral. The alopecia is apparent from birth in about a third of cases but may not be noted until later childhood. It has, rarely, been associated with phakomatosis pigmentovascularis. |
