Results 131 to 140 of about 5,055 (182)
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Keratoderma and spastic paralysis
British Journal of Dermatology, 1983Punctate keratoderma and spastic paralysis occurred in three generations of a family. Several members had keratoderma of the palms and soles or spastic paralysis or both. The family history was consistent with autosomal-dominant inheritance. The age at onset and the rate of progression of symptoms were variable.
F C, Powell +3 more
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Aquagenic palmoplantar keratoderma
Journal of the American Academy of Dermatology, 2001Aquagenic palmoplantar keratoderma is an acquired condition characterized by burning and edema limited to the hands after brief immersion in water. The 3 patients described possess a striking similarity to those with transient reactive papulotranslucent acrokeratoderma.
A C, Yan +6 more
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The inherited palmoplantar keratodermas
British Journal of Dermatology, 1997The inherited palmoplantar keratodermas (PPK) constitute a complex heterogeneous group of genodermatoses, which are difficult to classify clinically. The application of modern molecular biology techniques are leading to an increased understanding of the genetic bases of these disorders and are paving the way towards a classification based upon ...
R C, Ratnavel, W A, Griffiths
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Keratoderma palmoplantaris striata
Clinical and Experimental Dermatology, 1989A patient with keratoderma palmoplantaris striata is presented. In the family tree there are 36 relatives affected to a varying degree. The familial incidence is the largest reported in the literature reviewed. The response to etretinate was excellent, controlling the lesions with minimal side-effects.
CASADO, M. +5 more
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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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Palmoplantar Keratoderma with Amyotrophy
Dermatologica, 2009Four members of a South African Black family who have palmoplantar keratoderma with amyotrophy are reported. No neuromuscular defects have been found and the muscle thinning appears to result from disuse atrophy. Volar hyperhidrosis, nail abnormalities and in 2 cases knuckle pads, were additional features.
W K, Jacyk, P L, Bill
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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 palmo‐plantar 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, 1989Extensive 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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