Results 161 to 170 of about 81,034 (193)
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Epidermolysis Bullosa Simplex in the Collie Dog
Journal of the American Veterinary Medical Association, 1977SUMMARY Epidermolysis bullosa simplex was diagnosed in 4 Collie dogs. Three of the dogs were less than 6 months old when lesions were first noticed. Lesions were characterized by alopecia, erythema, edema, erythematous plaques, erosions, ulcers, crusts, atrophy, pigmentary changes, and (rarely) blisters affecting the skin over bony prominences and ...
D W, Scott, R D, Schultz
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Epidermolysis bullosa simplex with mottled pigmentation
British Journal of Dermatology, 1993A family in which epidermolysis bullosa simplex and mottled pigmentation are inherited as an autosomal dominant disorder is described. Clinical features include: non-scarring blistering, mainly affecting the limbs, mottled pigmentation, predominantly affecting the trunk and neck, warty hyperkeratotic papules of the palms and soles, small red scaly ...
R, Coleman, J I, Harper, B D, Lake
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Corneal Involvement in Epidermolysis Bullosa Simplex
Archives of Ophthalmology, 1980A 17-year-old boy and his mother represent the first reported cases of ocular (corneal) involvement of the simplex form of epidermolysis bullosa. Both had a ring-like configuration of fine bullous lesions in the midperiphery bilaterally at the level of deep corneal epithelium superficial to Bowman's membrane (basal cell layer), with the son manifesting
H, Granek, H P, Baden
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Epidermolysis bullosa simplex.
Cutis, 2003Blistering is a common occurrence generally caused by moderate or repetitive trauma to the skin. Blistering due to minor trauma is less common and may be associated with a group of heterogeneous genetic diseases called epidermolysis bullosa (EB). The level of vesiculation within the skin defines 3 major subtypes of EB: EB simplex (EBS), dystrophic EB ...
Jason F, Okulicz +2 more
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Expression signature of epidermolysis bullosa simplex
Human Genetics, 2011Epidermolysis bullosa simplex (EBS) is a skin disorder resulting from a weakened cytoskeleton of the proliferative compartment of the epidermis, leading to cell fragility and blistering. Although many mutations have been identified in intermediate filament keratins KRT5 and KRT14, detailed pathogenic mechanisms and the way these mutations affect cell ...
Mbarka, Bchetnia +8 more
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EPIDERMOLYSIS BULLOSA SIMPLEX IN TASMANIA
The Lancet, 1963D A, TILSLEY, T C, BEARD
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Proceedings of the 2nd International Conference on Tropical Medicine and Infectious Disease, 2019
Indra Wijaya +4 more
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Indra Wijaya +4 more
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Epidermolysis bullosa simplex (intraepidermal epidermolysis bullosa) and allied conditions
1990Thirty years before the rediscovery of Mendel’s laws of inheritance intraepidermal non-scarring blistering was called Erblichen Pemphigus by von Hebra [1]. Kobner in 1886 called the same condition epidermolysis bullosa hereditaria (EBH) [2]. Since the latter term soon became adopted for several congenital traumatic blistering diseases, Hallopeau [3 ...
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[Pretibial epidermolysis bullosa. A rare form of epidermolysis bullosa simplex].
Annales de dermatologie et de venereologie, 1998Pretibial epidermolysis bullosa had been classified as a rare localized form of autosomal dominant dystrophic epidermolysis bullosa.We report a sporadic case of a patient suffering from bullous lesions induced by minor trauma on pretibial skin. The lesions healed with atrophic scars. No milia formation was observed.
P, Tsianakas +5 more
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Treatment of epidermolysis bullosa simplex with dupilumab
The Journal of Dermatology, 2023Xiaofang Sun +3 more
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