Junctional epidermolysis bullosa inversa (Q103890)

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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.
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ID_1191822552
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    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.

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      CID11:ID_1191822552
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