Results 211 to 220 of about 4,210 (234)
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Hereditary Epidermolytic Palmoplantar Keratoderma
Archives of Dermatology, 1981We describe herein a patient in whose family 11 of 20 members have a palmoplantar keratoderma. The pathologic findings in the proband were those of epidermolytic hyperkeratosis. As in the other families described, the disease was found to be inherited as an autosomal dominant trait.
Robert L. Dimond +2 more
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A family with palmoplantar epidermolytic hyperkeratosis
Clinical and Experimental Dermatology, 1989Familial epidermolytic hyperkeratosis confined to the palms and soles was first characterized by Klaus and Weinstein in 1970. This entity has been the subject of only four subsequent reports. We report a family previously diagnosed as suffering from tylosis (Thost Unna syndrome), in which eleven members have been affected, and review the literature on ...
P.E. Hutchinson, J. Berth-Jones
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The American Journal of Dermatopathology, 2008
Hereditary skin diseases that are characterized ultrastructurally by intracellular clumpings of keratin tonofilaments, such as Darier disease and Ichthyosis Hystrix of Curth-Macklin, display epidermal dyskeratosis also histologically. Epidermolytic hyperkeratosis (EHK) and epidermolytic palmoplantar keratoderma (Voerner type) (EPPK) are 2 types of ...
Ziad Khamaysi +2 more
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Hereditary skin diseases that are characterized ultrastructurally by intracellular clumpings of keratin tonofilaments, such as Darier disease and Ichthyosis Hystrix of Curth-Macklin, display epidermal dyskeratosis also histologically. Epidermolytic hyperkeratosis (EHK) and epidermolytic palmoplantar keratoderma (Voerner type) (EPPK) are 2 types of ...
Ziad Khamaysi +2 more
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Epidermolytic Palmo‐plantar Keratoderma
International Journal of Dermatology, 1984ABSTRACT: An 11–year‐old girl who at 91/2 months was diagnosed as having keratoderma of the palms and soles, present since birth, developed typical granuloma annulare at the age of 11 years. To the authors’knowledge, this is the first report of epidermolytic palmo‐plantar keratoderma associated with granuloma annulare.
J R, Thomas, S L, Greene, W P, Su
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Nevoid Follicular Epidermolytic Hyperkeratosis
Archives of Dermatology, 1975Comedo-like follicular papules of hair-follicles, confined to the left side of the upper part of the body, were found in a 22-year-old woman. Histological features were of epidermolytic hyperkeratosis with involvement of the follicular epithelium and the sebaceous duct with compact hyperkeratosis, but almost no interfollicular epidermal alterations ...
Enno Christophers, Gerd Plewig
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European Journal of Medical Genetics, 2021
Epidermolytic ichthyosis and epidermolytic nevi share the same histopathological features of epidermolytic hyperkeratosis, characterized by distinctive vacuolar degeneration and hypergranulosis of the superficial epidermis. Both are caused by pathogenic variants in either of two keratin genes KRT1or KRT10, with epidermolytic ichthyosis presenting as a ...
Yi Zhao +7 more
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Epidermolytic ichthyosis and epidermolytic nevi share the same histopathological features of epidermolytic hyperkeratosis, characterized by distinctive vacuolar degeneration and hypergranulosis of the superficial epidermis. Both are caused by pathogenic variants in either of two keratin genes KRT1or KRT10, with epidermolytic ichthyosis presenting as a ...
Yi Zhao +7 more
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Epidermolytic Palmo‐plantar Keratoderma
International Journal of Dermatology, 1986An 11-year-old girl who at 9 1/2 months was diagnosed as having keratoderma of the palms and soles, present since birth, developed typical granuloma annulare at the age of 11 years. To the authors' knowledge, this is the first report of epidermolytic palmo-plantar keratoderma associated with granuloma annulare.
Eise van Dijk +3 more
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Nevus comedonicus with Epidermolytic Hyperkeratosis
Dermatology, 1987A 7-year-old girl had a linear nevus comedonicus affecting the right upper limb. Histologic examination of two biopsies specimens showed both the common changes of nevus comedonicus and the presence of epidermolytic hyperkeratosis. Therefore, nevus comedonicus should be included in the list of dermatoses having the distinctive histologic pattern of ...
A. Molinero, F.G. Aloi
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Persistent actinic epidermolytic hyperkeratosis
Journal of the American Academy of Dermatology, 1995Epidermolytic hyperkeratosis is a distinctive histologic change noted in a variety of acquired and congenital dermatoses. Its pathogenesis is unknown. We have observed acquired epidermolytic hyperkeratosis in four Japanese men.Our purpose was to report four cases of acquired epidermolytic hyperkeratosis induced by sun exposure.Four cases were studied ...
Tsukasa Takemura +3 more
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Management of Epidermolytic Ichthyosis in the Newborn
Neonatal Network, 2016AbstractEpidermolytic ichthyosis (EI) is a rare autosomal dominant genodermatosis that presents at birth as a bullous disease, followed by a lifelong ichthyotic skin disorder.1 Essentially, it is a defective keratinization caused by mutations of keratin 1 (KRT1) or keratin 10 (KRT10) genes, which lead to skin fragility, blistering, and eventually ...
Mondell Avril, Cheryl Riley
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