Genetically-determined epidermolysis bullosa (Q55769): Difference between revisions
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Epidermólise bolhosa (EB) é o nome dado a um grupo heterogêneo de afecções bolhosas que, na maioria dos casos, são decorrentes de defeitos geneticamente determinados em proteínas estruturais da epiderme e junção dermo-epidérmica. As formas genéticas devem ser distinguidas da doença imunobolhosa, epidermólise bolhosa acquisita (qv). | |||
| description / en | description / en | ||
Epidermolysis bullosa (EB) is the name given to a heterogeneous group of blistering disorders which in the majority of cases are due to genetically-determined defects in structural proteins of the epidermis and dermo-epidermal junction. The genetic forms are to be distinguished from the immunobullous disorder, epidermolysis bullosa acquisita (qv). | |||
Revision as of 03:26, 14 August 2026
Epidermolysis bullosa (EB) is the name given to a heterogeneous group of blistering disorders which in the majority of cases are due to genetically-determined defects in structural proteins of the epidermis and dermo-epidermal junction. The genetic forms are to be distinguished from the immunobullous disorder, epidermolysis bullosa acquisita (qv).
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1381715631 |
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| English | Genetically-determined epidermolysis bullosa |
Epidermolysis bullosa (EB) is the name given to a heterogeneous group of blistering disorders which in the majority of cases are due to genetically-determined defects in structural proteins of the epidermis and dermo-epidermal junction. The genetic forms are to be distinguished from the immunobullous disorder, epidermolysis bullosa acquisita (qv). |
