Epidermolysis bullosa simplex with mottled pigmentation (Q106961): Difference between revisions
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Epidermólise bolhosa simples com pigmentação mosqueada (EBS-MP) é um subtipo basal autossômico dominante de EBS devido a mutações no gene KRT5, que codifica a queratina 5. Caracteriza-se por bolhas generalizadas com pigmentação marrom mosqueada ou reticulada. | |||
| description / en | description / en | ||
Epidermolysis bullosa simplex with mottled pigmentation (EBS-MP) is an autosomal dominant basal subtype of EBS due to mutations in the KRT5 gene which encodes keratin 5. It is characterised by generalised blistering with mottled or reticulate brown pigmentation. | |||
Revision as of 13:57, 17 August 2026
Epidermolysis bullosa simplex with mottled pigmentation (EBS-MP) is an autosomal dominant basal subtype of EBS due to mutations in the KRT5 gene which encodes keratin 5. It is characterised by generalised blistering with mottled or reticulate brown pigmentation.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1688797966 |
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| English | Epidermolysis bullosa simplex with mottled pigmentation |
Epidermolysis bullosa simplex with mottled pigmentation (EBS-MP) is an autosomal dominant basal subtype of EBS due to mutations in the KRT5 gene which encodes keratin 5. It is characterised by generalised blistering with mottled or reticulate brown pigmentation. |
