Skin Fragility: Perspectives on Evidence-based Therapies
The term skin fragility disorders describes a group of conditions in which the structural integrity of the skin is compromised and its resistance to external shear forces diminished. Skin fragility can have different causes, ranging from genetic variations to inflammatory or physical phenomena. The...
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Society for Publication of Acta Dermato-Venereologica
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https://www.medicaljournals.se/acta/content/html/10.2340/00015555-3398
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doaj-f3bd2f1ca3c44699aa7d09a2841e15412020-11-24T21:47:14ZengSociety for Publication of Acta Dermato-VenereologicaActa Dermato-Venereologica0001-55551651-20572020-02-011005adv0005310.2340/00015555-33985661Skin Fragility: Perspectives on Evidence-based TherapiesLeena Bruckner-Tuderman0 The term skin fragility disorders describes a group of conditions in which the structural integrity of the skin is compromised and its resistance to external shear forces diminished. Skin fragility can have different causes, ranging from genetic variations to inflammatory or physical phenomena. The genetic skin fragility disorders, collectively called epidermolysis bullosa, serve as a paradigm for the study of causes and mechanisms of skin fragility. Recent biomedical research has revealed substantial genetic heterogeneity of the epidermolysis bullosa group, delivered ample new knowledge on its pathophysiology, and facilitated the design of evidence-based therapeutic strategies. The therapy development process extends from in vitro testing to preclinical validation in animal models, and clinical trials. This article reviews different approaches to curative and symptom-relief therapies, and appraises their status and perspectives for clinical implementation. https://www.medicaljournals.se/acta/content/html/10.2340/00015555-3398 skin blistering genodermatosis molecular therapy symptom-relief |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Leena Bruckner-Tuderman |
spellingShingle |
Leena Bruckner-Tuderman Skin Fragility: Perspectives on Evidence-based Therapies Acta Dermato-Venereologica skin blistering genodermatosis molecular therapy symptom-relief |
author_facet |
Leena Bruckner-Tuderman |
author_sort |
Leena Bruckner-Tuderman |
title |
Skin Fragility: Perspectives on Evidence-based Therapies |
title_short |
Skin Fragility: Perspectives on Evidence-based Therapies |
title_full |
Skin Fragility: Perspectives on Evidence-based Therapies |
title_fullStr |
Skin Fragility: Perspectives on Evidence-based Therapies |
title_full_unstemmed |
Skin Fragility: Perspectives on Evidence-based Therapies |
title_sort |
skin fragility: perspectives on evidence-based therapies |
publisher |
Society for Publication of Acta Dermato-Venereologica |
series |
Acta Dermato-Venereologica |
issn |
0001-5555 1651-2057 |
publishDate |
2020-02-01 |
description |
The term skin fragility disorders describes a group of conditions in which the structural integrity of the skin is compromised and its resistance to external shear forces diminished. Skin fragility can have different causes, ranging from genetic variations to inflammatory or physical phenomena. The genetic skin fragility disorders, collectively called epidermolysis bullosa, serve as a paradigm for the study of causes and mechanisms of skin fragility. Recent biomedical research has revealed substantial genetic heterogeneity of the epidermolysis bullosa group, delivered ample new knowledge on its pathophysiology, and facilitated the design of evidence-based therapeutic strategies. The therapy development process extends from in vitro testing to preclinical validation in animal models, and clinical trials. This article reviews different approaches to curative and symptom-relief therapies, and appraises their status and perspectives for clinical implementation. |
topic |
skin blistering genodermatosis molecular therapy symptom-relief |
url |
https://www.medicaljournals.se/acta/content/html/10.2340/00015555-3398
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work_keys_str_mv |
AT leenabrucknertuderman skinfragilityperspectivesonevidencebasedtherapies |
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1725898438165397504 |