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Nailfold capillaroscopic changes in Kindler syndrome
Kindler syndrome (KS), the fourth major type of hereditary epidermolysis bullosa (HEB), is a rare, autosomal recessive disorder characterized by skin fragility and blistering at birth followed by development of marked photosensitivity and progressive poikilodermatous skin changes in later years. We...
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| Publicado no: | Intractable Rare Dis Res |
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| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
International Research and Cooperation Association for Bio & Socio-Sciences Advancement
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4660865/ https://ncbi.nlm.nih.gov/pubmed/26668784 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5582/irdr.2015.01038 |
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