Results 31 to 40 of about 2,889 (186)
Disseminated Erythema and Vesicles on the Trunk and Extremities in a Teenager: A Quiz [PDF]
Acta Dermato-VenereologicaChunxia Zhao, Hua Wang, Lei Wang
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Familial epidermolysis bullosa acquisita
Dermatology Online Journal, 2008 Epidermolysis bullosa acquisita (EBA) is an acquired blistering skin disorder caused by IgG autoantibodies directed against type VII collagen. In contrast to the genetic forms of epidermolysis bullosa, EBA is usually an acquired, sporadic disease. In this report, we describe a family with two cases of EBA in an uncle-nephew pair, and a third family ...
Noe, Megan H +3 more
openaire +4 more sources
High-Affinity Binding of the NC1 Domain of Collagen VII to Laminin 5 and Collagen IV [PDF]
, 2006 Anchoring functions of collagen VII depend on its ability to form homotypic fibrils and to bind to other macromolecules to form heterotypic complexes. Biosensor-based binding assays were employed to analyze the kinetics of the NC1 domain-mediated binding
Brittingham, Raymond +2 more
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Diseases presenting with vesicular and erosive lesions of oral mucous membranes
Przegląd Dermatologiczny, 2017 Disorders of the oral mucosa are an area of interdisciplinary cooperation involving physicians from a diverse range of medical specialties.
Kamila Ociepa, Agnieszka Żebrowska
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Generalized erosions, blisters, scarring, and milia in a 65-year-old woman: a diagnostic challenge
Journal of the Egyptian Women’s Dermatologic Society, 2021 Epidermolysis bullosa acquisita (EBA) is a chronic autoimmune subepidermal blistering disease of the skin and mucous membranes. EBA is caused by antibodies targeting type VII collagen, the major component of anchoring fibrils that connects the basement ...
Galal El Enany +8 more
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Cutaneous Manifestations in Inflammatory Bowel Diseases [PDF]
, 2015 Inflammatory bowel diseases have a high frequency in Europe. They are chronic disorders that evolve with relapses and remissions. Clinical features include the signs of underlying inflammatory bowel disease and also signs of extraintestinal ...
Benea, Vasile +6 more
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An 81-Year-Old Woman with Recalcitrant Blisters
Dermatopathology, 2018 Epidermolysis bullosa acquisita (EBA) is a rare mucocutaneous blistering disorder with typical onset in adulthood. Diagnosis and management can be difficult owing to the variability in presentation and clinical manifestation.
Daniel C. Butler
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Pemphigoid diseases in infancy and childhood. A review of the literature
Przegląd Dermatologiczny, 2023 Bullous pemphigoid is an autoimmune blistering disease that very rarely affects children. Clinical differences in locations of skin lesions led to the distinction of infantile versus childhood pemphigoid. Mucous membranes can be affected.
Magdalena Jałowska +2 more
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Angina bullosa hemorrhagica an enigmatic oral disease [PDF]
, 2015 Angina bullosa hemorrhagica (ABH) is an enigmatic oral disorder described for the first time by Badham in 1967 to define blisters with a hematic content in the oral cavity and oropharynx unrelated to any hematological, dermatological or systemic ...
Aguirre-Urizar, Jose Manuel +3 more
core +1 more source
Acta Dermato-Venereologica, 2018 Circulating anti-type VII collagen autoantibodies are frequently detected in patients with recessive dystrophic epidermolysis bullosa (RDEB). However, evidence supporting their pathogenic role in inducing epidermolysis bullosa acquisita (EBA) has been ...
Liliana Guerra +6 more
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