Junctional epidermolysis bullosa inversa (Q103890): Difference between revisions
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Epidermólise bolhosa juncional inversa é um subtipo grave raro de epidermólise bolhosa juncional, caracterizado por bolhas e erosões confinadas às áreas intertriginosas da pele, ao esôfago e à vagina. | |||
| description / en | description / en | ||
Junctional epidermolysis bullosa inversa is a rare severe subtype of junctional epidermolysis bullosa, characterised by blistering and erosions confined to intertriginous skin sites, the oesophagus, and vagina. | |||
Revision as of 09:40, 17 August 2026
Junctional epidermolysis bullosa inversa is a rare severe subtype of junctional epidermolysis bullosa, characterised by blistering and erosions confined to intertriginous skin sites, the oesophagus, and vagina.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1191822552 |
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| English | Junctional epidermolysis bullosa inversa |
Junctional epidermolysis bullosa inversa is a rare severe subtype of junctional epidermolysis bullosa, characterised by blistering and erosions confined to intertriginous skin sites, the oesophagus, and vagina. |
