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Acral peeling skin syndrome in two East-African siblings: case report
BACKGROUND: Acral peeling skin syndrome is a rare autosomal recessive genodermatosis due to a missense mutation in transglutaminase 5. The skin peeling occurs at the separation of the stratum corneum from the stratum granulosum. CASE PRESENTATION: We present a case of two siblings who developed cont...
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| Hoofdauteurs: | , , , |
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| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
BioMed Central
2012
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3341202/ https://ncbi.nlm.nih.gov/pubmed/22429841 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-5945-12-2 |
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