Poikiloderma (Q62989): Difference between revisions
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Poiquilodermia é definida como uma combinação de atrofia da pele, pigmentação e telangiectasias. É um componente de uma série de síndromes genéticas, de determinados transtornos autoimunes sistêmicos não específicos de órgãos, e pode ocorrer subsequente a lesão na pele, incluindo por radioterapia. | |||
| description / en | description / en | ||
Poikiloderma is defined as a combination of skin atrophy, pigmentation and telangiectasia. It is a component of a number of genetic syndromes, of certain non-organ-specific systemic autoimmune disorders and may follow skin injury including from radiotherapy. | |||
Revision as of 10:28, 14 August 2026
Poikiloderma is defined as a combination of skin atrophy, pigmentation and telangiectasia. It is a component of a number of genetic syndromes, of certain non-organ-specific systemic autoimmune disorders and may follow skin injury including from radiotherapy.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_657613175 |
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| English | Poikiloderma |
Poikiloderma is defined as a combination of skin atrophy, pigmentation and telangiectasia. It is a component of a number of genetic syndromes, of certain non-organ-specific systemic autoimmune disorders and may follow skin injury including from radiotherapy. |
