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Clinical management for epidermolysis bullosa dystrophica [PDF]
, 2008 Epidermolysis bullosa (EB) consists of a group of genetic hereditary disorders in which patients frequently present fragile skin and mucosa that form blisters following minor trauma.
CANDIDO, Liliani A. +4 more
core +3 more sources
Inherited epidermolysis bullosa [PDF]
Orphanet Journal of Rare Diseases, 2010 Inherited epidermolysis bullosa (EB) encompasses a number of disorders characterized by recurrent blister formation as the result of structural fragility within the skin and selected other tissues. All types and subtypes of EB are rare; the overall incidence and prevalence of the disease within the United States is approximately 19 per one million live
openaire +3 more sources
Epidermolysis Bullosa Acquisita: The 2019 Update
Frontiers in Medicine, 2019 Epidermolysis bullosa acquisita (EBA) is an orphan autoimmune disease. Patients with EBA suffer from chronic inflammation as well as blistering and scarring of the skin and mucous membranes.
H. Koga +5 more
semanticscholar +1 more source
Lethal acantholytic epidermolysis bullosa
Definitions, 2020 Lethal acantholytic epidermolysis bullosa is a suprabasal subtype of epidermolysis bullosa simplex (EBS, see this term) characterized by generalized oozing erosions, usually in the absence of blisters.
semanticscholar +1 more source
JEADV Clinical Practice, EarlyView.Capsule Summary Bruxism and sweat‐induced facial blisters can affect patients with Recessive Dystrophic Epidermolysis Bullosa (RDEB) quality of life (QoL). We present the outcomes of orofacial BTX‐A infiltrations to treat these conditions. Three patients with severe RDEB, bruxism and microstomia received BTX‐A infiltrations (50U‐100U) in masseters and ...
Susanne Krämer +4 more
wiley +1 more source
Prevalence and molecular genetic features of epidermolysis bullosa in Krasnodar Krai
Кубанский научный медицинский вестник, 2020 Background. Epidermolysis bullosa defi nes a clinically and genetically heterogeneous group of severe orphan disorders manifested with a congenital propensity for bullae (blisters) propagation on skin and mucous membranes of oesophagus, intestine ...
I. I. Pavlyuchenko +3 more
doaj +1 more source
Physical Development and Puberty in Related Patients with Kindler Epidermolysis Bullosa: Case Study
Вопросы современной педиатрии, 2022 Background. Kindler epidermolysis bullosa is orphan, autosomal recessive disease and it is one of the variants of congenital epidermolysis bullosa. Its severe course is characterized by high risk of multifactorial malnutrition, chronic inflammation due ...
Maria A. Leonova +3 more
doaj +1 more source
Proceedings of the National Academy of Sciences of the United States of America, 2019 Significance This study demonstrates a therapeutic option using induced pluripotent stem cells (iPSCs), gene editing, and tissue engineering techniques for the development of a long-lasting treatment that will result in the permanent closure of ...
J. Jacków +11 more
semanticscholar +1 more source
JCI Insight, 2019 BACKGROUNDRecessive dystrophic epidermolysis bullosa (RDEB) patients have mutations in the COL7A1 gene and thus lack functional type VII collagen (C7) protein; they have marked skin fragility and blistering. This single-center phase 1/2a open-label study
S. Eichstadt +17 more
semanticscholar +1 more source
Australian Veterinary Journal, EarlyView.Pyrexia is a non‐specific clinical sign associated with many diseases in dogs. This case series examines the final diagnoses, breed distribution and outcomes in dogs aged 18 months or under with pyrexia >24 h duration. Medical record databases of 11 Australian emergency and referral hospitals between 1st January 2020 and 31st January 2025 were searched
H Lobegeier +3 more
wiley +1 more source