Results 51 to 60 of about 81,034 (193)
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
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
doaj +1 more source
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
doaj +1 more source
Validation of the Investigator's Global Assessment Scale for Epidermolysis Bullosa Simplex
JEADV Clinical Practice, EarlyView.ABSTRACT Background There is a lack validated outcome measures to assess wound severity in epidermolysis bullosa simplex (EBS). Objectives To assess the reliability and validity of the Investigator's Global Assessment (IGA) scale and a newly developed palms/soles subscale through in‐clinic scoring and review of patient‐submitted photographs.
Pirunthan Pathmarajah +13 more
wiley +1 more source
Australasian Journal of Dermatology, EarlyView.ABSTRACT Epidermolysis bullosa (EB) is an inherited mechanobullous genodermatosis caused by a mutation in genes encoding proteins integral to skin integrity. Premature termination codon readthrough therapies, such as gentamicin, have promise in facilitating full‐length protein expression in patients with EB.
Kelvin Truong +4 more
wiley +1 more source
Expert consensus on oral management in autoimmune bullous diseases, erythema multiforme and SJS/TEN
Journal of the European Academy of Dermatology and Venereology, EarlyView.This international Delphi study achieved expert consensus on 58 statements guiding the management of oral involvement in autoimmune bullous diseases, erythema multiforme and SJS‐TEN. The recommendations emphasize multidisciplinary care, oral hygiene and tailored topical, systemic and inpatient oral management.
Shalini Nayee +39 more
wiley +1 more source
Gene expression analysis of epidermolysis bullosa simplex with mottled pigmentation
, 2013 Epidermolysis bullosa simplex with mottled pigmentation (EBS-MP) is a subtype of epidermolysis bullosa simplex first reported in 1979. The disease has its onset in early childhood and manifests with either much localized skin blistering, resembling the ...
Lacroix, Jacynthe +9 more
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Genetic Bases of Epidermolysis Bullosa Simplex and Epidermolytic Hyperkeratosis [PDF]
, 1994 Keratins are the major structural proteins of the epidermis. Analyzing keratin gene sequences, appreciating the switch in keratin gene expression that takes place as epidermal cells commit to terminally differentiate, and elucidating how keratins ...
Hutton, Elizabeth +9 more
core +1 more source
Localized epidermolysis bullosa simplex with generalized enamel hypoplasia in a child
, 2006 Epidermolysis bullosa is an uncommon disease characterized by the formation of blisters following minor trauma. The three major types are simplex, junctional, and dystrophic.
HATİPOĞLU, HASAN +2 more
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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