EB (epidermolysis bullosa)-House Austria: Pioneering work for the care of patients with rare diseases
Autor: | Martin Laimer, Johann W. Bauer, Helmut Hintner, Christine Prodinger |
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Rok vydání: | 2020 |
Předmět: |
medicine.medical_specialty
EB - Epidermolysis bullosa business.industry Dermatology Disease medicine.disease Clinical study 030207 dermatology & venereal diseases 03 medical and health sciences 0302 clinical medicine Rare Diseases Family medicine Austria medicine Outpatient clinic Humans Epidermolysis bullosa Patient group business Epidermolysis Bullosa Skin |
Zdroj: | Journal der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDGReferences. 18(11) |
ISSN: | 1610-0387 |
Popis: | The care of patients with epidermolysis bullosa (EB) poses a major challenge due to the rarity, heterogeneity and complexity of the disease as well as the occurrence of numerous primary and secondary extracutaneous manifestations, causing a significant morbidity and mortality. Specialized treatment centers are essential for offering these patients adequate care, including individual, interdisciplinary coordinated treatments according to current medical standards, and access to innovative therapeutic options. Against this background, the EB House Austria was founded in 2005 and designated the first national center of expertise for genodermatoses with a focus on EB in 2017. In the same year, it became a member of the European Reference Network for Rare Skin Diseases (ERN Skin). The pillars of this institution (outpatient clinic, research unit, academy, clinical study center) interact closely with each other, with numerous national and international clinical and scientific partners, as well as with patients and their relatives via the DEBRA Austria patient group. The development of the EB House Austria as a reference center is characterized by a long-term pioneering work, which in turn could pave the way for the optimization of care for comparable diseases as well as general care structures. |
Databáze: | OpenAIRE |
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