نتایج جستجو برای: blistering skin disease

تعداد نتایج: 1643649  

Journal: :Dermatology Reports 2023

Pemphigus vulgaris (PV) is an autoimmune blistering disease affecting the skin and mucosa. It clinically presents as painful erosions, mainly in oral cavity, flaccid blisters erosions on skin. Steven-johnson syndrome/toxic epidermal necrolysis (SJS/TEN) a severe mucocutaneous drug hypersensitivity reaction characterized by painful, dusky, erythematous eruptions that often progress to blisters, ...

Journal: :Indian journal of dermatology, venereology and leprology 1998
P K Kaviarasan P V S Prasad Shradda P Viswanathan

Kindler syndrome is a rare autosomal recessive disorder associated with skin fragility. It is characterized by blistering in infancy, photosensitivity and progressive poikiloderma. The syndrome involves the skin and mucous membrane with radiological changes. The genetic defect has been identified on the short arm of chromosome 20. This report describes an 18-year-old patient with classical feat...

Journal: :Case reports in gastrointestinal medicine 2021

Pemphigus vulgaris (PV) is an autoimmune blistering disorder of the skin and mucosal surfaces characterized by acantholysis (loss adhesion between epidermal cells). Esophageal involvement PV underdiagnosed entity as routine diagnostic endoscopy not recommended in asymptomatic patients. Dysphagia odynophagia are common presenting symptoms; however, upper gastrointestinal bleeding (UGIB) associat...

2010
Radhika Ganeshan Jiangli Chen Peter J. Koch

Genetically engineered mice have been essential tools for elucidating the pathological mechanisms underlying human diseases. In the case of diseases caused by impaired desmosome function, mouse models have helped to establish causal links between mutations and disease phenotypes. This review focuses on mice that lack the desmosomal cadherins desmoglein 3 or desmocollin 3 in stratified epithelia...

2016
A. Dubois M. Arefi M. P. Splitt S. Leech S. Natarajan N. Rajan

A 5-year-old boy presented with a history of dry scaly skin. He had been born at term, with no collodion membrane or erythroderma noted at delivery. Skin changes were noted soon after birth, with widespread dryness and occasional blistering, mainly affecting the toes. Previous treatment with emollients and topical corticosteroids had not resulted in improvement. There was no family history of d...

2015
Allison J Cowin

Inherited skin fragility disorders comprise a group of disorders, mainly designated as epidermolysis bullosa (EB), that are characterised by mechanical induced blistering and erosions of the skin and mucous membranes caused by mutations of gene coding for protein components of the dermal–epidermal junction zone. Patients with EB experience various degrees of recurrent skin blistering, widesprea...

Journal: :AJP reports 2016
Hiroyuki Wakiguchi Shunji Hasegawa Shinji Maeba Sasagu Kimura Satoko Ito Hiroshi Tateishi Kazuhiro Ueda Shouichi Ohga

Background Epidermolysis bullosa simplex (EBS) is a rare genodermatosis resulting from multiple gene mutations, including KRT5 and KRT14. The clinical expression of the mechanobullous skin fragility disease has not been fully explained by the genotype. Case Description An 11-day-old Japanese newborn infant was hospitalized because of herpetiform skin blistering on the feet, which expanded syste...

Journal: : 2023

Staphylococcal-scalded skin syndrome (SSSS) is a widespread, scaly erythematous condition caused by the exfoliative toxin of Staphylococcus aureus. This disease usually affects children under 5 years age with common symptoms scabbing and blistering, which often responds quickly to antibiotic therapy. The authors reported 4 cases SSSS, all identified as 2 admitted at Hai Phong Children Hospital....

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