Epidermolysis bullosa hereditaria simplex
Identifieur interne : 003D61 ( Main/Exploration ); précédent : 003D60; suivant : 003D62Epidermolysis bullosa hereditaria simplex
Auteurs : Eberhard Passarge [États-Unis]Source :
- The Journal of Pediatrics [ 0022-3476 ] ; 1965.
English descriptors
- Teeft :
- Bulla, Bullosa, Dermat, Dystrophic, Dystrophic changes, Dystrophic forms, Epidermolysis, Epidermolysis bullosa, Epidermolysis bullosa hereditaria, Epidermolysis bullosa hereditaria letalis, Epidermolysis bullosa hereditaria simplex, Hereditaria, Mild trauma, Mucous membranes, Nikolsky sign, Propositus, Recessive, Schnyder, Simple form, Simplex, Syph, Trauma.
Abstract
This paper describes a kindred affected with epidermolysis bullosa hereditaria simplex in 4 generations. The absence of dystrophic changes of the skin and mucous membranes is characteristic of this type and gives a better prognosis than the dystrophic forms.
Url:
DOI: 10.1016/S0022-3476(65)80372-9
Affiliations:
Links toward previous steps (curation, corpus...)
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- to stream Istex, to step Checkpoint: 002A83
- to stream Main, to step Merge: 003E48
- to stream Main, to step Curation: 003D61
Le document en format XML
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<term>Dystrophic forms</term>
<term>Epidermolysis</term>
<term>Epidermolysis bullosa</term>
<term>Epidermolysis bullosa hereditaria</term>
<term>Epidermolysis bullosa hereditaria letalis</term>
<term>Epidermolysis bullosa hereditaria simplex</term>
<term>Hereditaria</term>
<term>Mild trauma</term>
<term>Mucous membranes</term>
<term>Nikolsky sign</term>
<term>Propositus</term>
<term>Recessive</term>
<term>Schnyder</term>
<term>Simple form</term>
<term>Simplex</term>
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<front><div type="abstract" xml:lang="en">This paper describes a kindred affected with epidermolysis bullosa hereditaria simplex in 4 generations. The absence of dystrophic changes of the skin and mucous membranes is characteristic of this type and gives a better prognosis than the dystrophic forms.</div>
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