Results 171 to 180 of about 8,647 (203)
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Acquired Palmoplantar Keratoderma
American Journal of Clinical Dermatology, 2007Palmoplantar keratodermas (PPKs) are a diverse entity of disorders that are characterized by abnormal thickening of the skin on the palms and soles. Traditionally they have been classified as either hereditary or acquired and are distinguished from each other on the basis of mode of inheritance, presence of transgrediens (defined as contiguous ...
Shaily, Patel +2 more
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Clinical and Experimental Dermatology, 1988
Summary Skin changes are nearly always found in myxoedema. 1 Scalp hair may be coarse, dry and sparse, the face, and hands puffy with a pasty-yellow complexion. Commonly the skin of the limbs is dry to the touch and may crack and redden over the shins (eczema craquele). 2 The nails may be brittle.
J M, Good +3 more
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Summary Skin changes are nearly always found in myxoedema. 1 Scalp hair may be coarse, dry and sparse, the face, and hands puffy with a pasty-yellow complexion. Commonly the skin of the limbs is dry to the touch and may crack and redden over the shins (eczema craquele). 2 The nails may be brittle.
J M, Good +3 more
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Circumscribed Palmoplantar Keratoderma
Australasian Journal of Dermatology, 1970SUMMARYA case of focal tender thickening of the palms and soles, with associated abnormalities of the cornea, is described. It is believed to be an example of circumscribed palmoâplantar keratoderma, of autosomal recessive inheritance. Possible mechanisms involved in the production of the lesions are considered, and an approach to treatment discussed.
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Punctate Porokeratotic Keratoderma
Archives of Dermatology, 1973Extensive review of published reports of punctate keratoderma has revealed only one similar case to that reported in the present paper. This represents a diffuse involvement of the palms and soles with pinpoint keratotic plugs and pits which were proven to be parakeratotic columns histologically identical with the cornoid lamellae of porokeratotic ...
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Hereditary Palmoplantar Keratodermas
JDDG: Journal der Deutschen Dermatologischen Gesellschaft, 2009SummaryHereditary palmoplantar keratodermas (PPK) comprise a clinically and genetically heterogeneous group of genodermatoses, which share impaired epidermal differentiation resulting in prominent palmoplantar hyperkeratosis. Classically, keratodermas have been separated according to their clinical appearance into diffuse, focal, and as a feature of ...
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Punctuate porokeratotic keratoderma.
Archives of dermatology, 1988Two unrelated patients had numerous palmoplantar "music box spine" keratotic plugs and pits of 11 and 13 years' duration. Histologic examination revealed a compact column of parakeratosis resembling that of a cornoid lamella of porokeratotic conditions. Ultrastructurally in clinically affected skin, the stratum corneum contained numerous variable-sized
S J, Friedman +3 more
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Journal of the American Medical Association, 1934
Keratoderma blennorrhagicum is an interesting dermatosis associated with gonorrheal arthritis and occurs almost exclusively in the male sex, although three cases have been reported in females by Lees, 1 Issac 2 and Robert. 3 It occurs at all ages, and probably more frequently than the literature shows, because it is unrecognized in the very mild types.
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Keratoderma blennorrhagicum is an interesting dermatosis associated with gonorrheal arthritis and occurs almost exclusively in the male sex, although three cases have been reported in females by Lees, 1 Issac 2 and Robert. 3 It occurs at all ages, and probably more frequently than the literature shows, because it is unrecognized in the very mild types.
openaire +1 more source