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Congenital facial linear porokeratosis
Clinical and Experimental Dermatology, 2005We report a unique case of congenital linear porokeratosis with exclusive facial involvement in a 27-year-old Chinese man. No other family member was affected. To our knowledge, this is the first report in the English literature of congenital linear porokeratosis confined to the face.
Z H, Zhang +4 more
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Linear porokeratosis of Mibelli and DSAP
Clinical and Experimental Dermatology, 1986Summary Linear porokeratosis and disseminated superficial actinic porokeratosis (DSAP) are clinical variants of porokeratosis. We report the rare coexistence of these two variants. Porokeratosis is a genodermatosis which has at least five different clinical variants; Mibelli, linear, DSAP, plantaris palmaris et disseminata, and punctate (Wade
J S, Dover, J A, Miller, G M, Levene
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Generalized Linear Porokeratosis
Journal of Cutaneous Medicine and Surgery, 2022Yang Lu, Lin Feng
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European Journal of Pediatric Dermatology, 2016
The basonuclin, a gene mapped in 15q25.1- position 26.1, has been identified in familial forms of porokeratosis. Linear porokeratosis, which is often distributed along the lines of Blaschko, is a form of nevic porokeratosis, probably related to a post-zygotic mutation resulting in mosaicism.
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The basonuclin, a gene mapped in 15q25.1- position 26.1, has been identified in familial forms of porokeratosis. Linear porokeratosis, which is often distributed along the lines of Blaschko, is a form of nevic porokeratosis, probably related to a post-zygotic mutation resulting in mosaicism.
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Pediatric Dermatology, 2000
Abstract: Porokeratosis is a genodermatosis characterized by abnormal epidermal keratinization with the histologic finding of cornoid lamella. To date, five clinical variants have been identified. However, the coexistence of these variants in a single patient has been described only rarely.
D H, Suh +5 more
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Abstract: Porokeratosis is a genodermatosis characterized by abnormal epidermal keratinization with the histologic finding of cornoid lamella. To date, five clinical variants have been identified. However, the coexistence of these variants in a single patient has been described only rarely.
D H, Suh +5 more
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Linear Porokeratosis in a Family With DSAP
Archives of Dermatology, 1972To the Editor.— Recent letters have argued the merits of lumping vs splitting in porokeratosis (Porokeratosis, LETTERS TO THE EDITOR. Arch Derm 105:296, 1972). Here presented is some evidence for lumping. This 36-year-old woman developed a linear porokeratosis at age 5 following the measles (Fig 1).
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Linear Porokeratosis and Other Linear Cutaneous Eruptions of Childhood
Archives of Pediatrics & Adolescent Medicine, 1979Several distinct linear cutaneous eruptions occur in childhood. They differ in natural history, response to therapy, and association with other abnormalities that may affect the child's general well-being.
G F, Cox, M, Jarratt
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[Porokeratosis linearis unilateralis (linear porokeratosis)].
Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete, 1986A case of linear porokeratosis is reported. This rare disease is described and the different entities that can be grouped under the term porokeratosis are discussed.
H P, Apel, A, Kuhlwein, M, Jänner
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