Results 31 to 40 of about 2,415 (163)
Epidermolysis Bullosa in Newborn: A Rare Case with Management Dilemmas [PDF]
Journal of Clinical and Diagnostic Research, 2020 Epidermolysis Bullosa (EB) is a rare genetic and connective tissue disorder affecting 1 in every 50000 live birth that causes skin to be very fragile and blister easily.
Ekta Kale, Sumita Mehta, Tarun Kumar
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Reproductive alternatives for patients with dystrophic epidermolysis bullosa
Einstein (São Paulo)Epidermolysis bullosa describes a group of skin conditions caused by mutations in genes encoding proteins related to dermal-epidermal adhesion. In the United States, 50 cases of epidermolysis bullosa per 1 million live births are estimated, 92% of which ...
Denise Maria Christofolini +8 more
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Otorhinolaryngological and esophageal manifestations of epidermolysis bullosa
Brazilian Journal of Otorhinolaryngology, 2008 Summary: Epidermolysis bullosa (EB) is a group of skin diseases with different clinical manifestations and varied inheritance patterns. Blisters may appear spontaneously or following minimal trauma to the skin or mucosa.
Rodrigo Santana Fantauzzi +5 more
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MMP-9 and CXCL8/IL-8 are potential therapeutic targets in epidermolysis bullosa simplex.
PLoS ONE, 2013 Epidermolysis bullosa refers to a group of genodermatoses that affects the integrity of epithelial layers, phenotypically resulting in severe skin blistering. Dowling-Meara, the major subtype of epidermolysis bullosa simplex, is inherited in an autosomal
Thomas Lettner +5 more
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Anais Brasileiros de Dermatologia, 2011 Lesões melanocíticas adquiridas assemelhando-se à melanoma têm sido descritas nos principais grupos da Epidermólise bolhosa, e referidas como "Nevos da Epidermólise bolhosa''.
Carolina Porto Cotrim +5 more
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Frontiers in Pediatrics, 2023 ObjectiveThis article aims to explore the diagnosis, molecular characteristics, treatment, and prognosis of epidermolysis bullosa with pyloric atresia (EB-PA).MethodsThe clinical manifestations, diagnosis and treatment, and genetic characteristics of a ...
Caiyun Luo +7 more
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Darier disease—A review highlighting new insights from the Darier Disease International Task Force
Journal of the European Academy of Dermatology and Venereology, EarlyView.This review provides a global, clinically focused overview of DD, detailing cutaneous and extracutaneous manifestations, disease classification and severity scoring. It emphasizes early recognition, multidisciplinary management and practical guidance for dermatologists to apply evidence‐based care in diverse skin phototypes. Abstract Darier disease (DD)
Sofia Labbouz +49 more
wiley +1 more source
Increased Genetic Instability in Exfoliated Oral Cells in Patients With Epidermolysis Bullosa
Oral Diseases, EarlyView.ABSTRACT Objective To analyze the nuclear abnormalities of cytotoxicity—karyorrhexis (KR), karyolysis (KL), and pyknosis (PN)—and genotoxicity—micronucleus (MN) in exfoliated cells from different sites of the oral mucosa in patients with Epidermolysis Bullosa (EB) and a control group.
Ana Carolina Sias Franco Franzosi +5 more
wiley +1 more source
Pediatric Dermatology, EarlyView.ABSTRACT Background/Objectives Pediatric patients with epidermolysis bullosa (EB) experience lifelong complications, and wound healing is an important treatment goal. In the phase III EASE study (NCT03068780), Oleogel‐S10 accelerated wound healing in EB.
Eli Sprecher +16 more
wiley +1 more source
Archives of Dermatology, 1983 • Two patients with a new mechanobullous disease are described. The trauma-induced bullae were present at birth. The nails were deformed in both cases. Both patients were isolated cases; so far, the inheritance pattern is not known. The histologic picture was unique.
P K, Jain, A, Kaushik
openaire +3 more sources