Informace o publikaci
Ten years of DNA diagnostics of epidermolysis bullosa in the Czech Republic
| Autoři | |
|---|---|
| Rok publikování | 2016 |
| Druh | Článek v odborném periodiku |
| Časopis / Zdroj | British Journal of Dermatology |
| Fakulta / Pracoviště MU | |
| Citace | |
| www | http://onlinelibrary.wiley.com/doi/10.1111/bjd.14370/epdf |
| Doi | http://dx.doi.org/10.1111/bjd.14370 |
| Obor | Dermatovenerologie |
| Klíčová slova | PEELING SKIN SYNDROME; MUTATIONS; CLASSIFICATION; SIMPLEX; GENE |
| Přiložené soubory | |
| Popis | Epidermolysis bullosa (EB) is a heterogeneous group of inherited skin disorders characterized by blister formation. Classification of patients with EB begins with their separation into one of the four major EB groups, based on the level to which blisters develop: EB simplex (EBS), junctional EB (JEB), dystrophic EB (DEB) and Kindler syndrome. The next level of subclassification takes into account the clinical features present in a given patient, most notably the distribution and severity of cutaneous and extracutaneous disease involvement. |
| Související projekty: |