2008
DOI: 10.1016/j.jaad.2008.02.004
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The classification of inherited epidermolysis bullosa (EB): Report of the Third International Consensus Meeting on Diagnosis and Classification of EB

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Cited by 827 publications
(904 citation statements)
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“…2A) (23), we anticipated a potentially greater contribution of BM-derived cells in the regenerating epithelia of the engrafted Col 7-null mouse skin. The engrafted Col 7-null mouse skin initially showed extensive subepidermal detachment, similar to the skin pathology seen in human patients with RDEB (21). At 4 wk after the engraftment, we noted an even greater contribution of GFP-positive cells expressing keratinocytespecific keratins in the regenerating epidermis and hair follicles of the engrafted Col 7-null mouse skin (Fig.…”
Section: Resultssupporting
confidence: 74%
“…2A) (23), we anticipated a potentially greater contribution of BM-derived cells in the regenerating epithelia of the engrafted Col 7-null mouse skin. The engrafted Col 7-null mouse skin initially showed extensive subepidermal detachment, similar to the skin pathology seen in human patients with RDEB (21). At 4 wk after the engraftment, we noted an even greater contribution of GFP-positive cells expressing keratinocytespecific keratins in the regenerating epidermis and hair follicles of the engrafted Col 7-null mouse skin (Fig.…”
Section: Resultssupporting
confidence: 74%
“…Examples are the PPKs, which sometimes show nonacral involvement, eg, Vohwinkel keratoderma 127 caused by a particular dominant GJB2 mutation (connexin 26), 128 Mal de Meleda 129 caused by recessive SLURP1 mutations, 130 and Papillon-Lefèvre syndrome 131 caused by recessive CTSC mutations encoding cathepsin C. 132 Mutations in keratin 5 or 14 cause epidermolysis bullosa simplex, 133,134 which can present with severe neonatal blistering clinically indistinguishable from EI. 62,65,135 Importantly, hypohidrosisea common symptom in ichthyoses, especially ARCI 136 erepresents one main criterion for the heterogeneous group of the ectodermal dysplasia. 137,138 Generalized erythroderma with scaling, and even collodion membranes, have been described in single cases of hypohidrotic ectodermal dysplasia.…”
Section: Other Diseases Considered In the Classification Of Inheritedmentioning
confidence: 99%
“…Kindler syndrome has only recently been added as part of the classification of EB 58 . Only few case reports of patients with Kindler syndrome describe their oral features 34,[85][86][87][88][89][90] .…”
Section: Kindler Syndromementioning
confidence: 99%
“…Classification schemes were first introduced by Pearson in 1962 92 . Since then, various consensus classifications have been published 58,93,94 .…”
Section: General Information On Epidermolysis Bullosamentioning
confidence: 99%
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