نتایج جستجو برای: keratoderma

تعداد نتایج: 755  

Journal: :Dermatology online journal 2000
Arielle Nagler Kevin P Boyd Rishi R Patel Hyun-soo Lee

We present a case of a 48-year-old man with an approximately 30-year history of spiny projections on the palms, which were histopathologically consistent with spiny keratoderma. Spiny keratoderma is a rare entity of unknown etiology that has been described with both hereditary and acquired variants. The hereditary form, which is most likely the diagnosis in our patient, manifests at a younger a...

Journal: :Case Reports 2013

Journal: :BMJ Case Reports 2017

2016
Anne Bruun Krøigård Liv Eline Hetland Ole Clemmensen Diana C. Blaydon Jens Michael Hertz Anette Bygum

BACKGROUND An autosomal dominant form of diffuse non-epidermolytic palmoplantar keratoderma, palmoplantar keratoderma of Bothnian type, is caused by mutations in the AQP5 gene encoding the cell-membrane water channel protein aquaporin 5 leading to defective epidermal-water-barrier function in the epidermis of the palms and soles. CASE PRESENTATION We report the first Danish family diagnosed w...

2003
Gisele Viana de Oliveira Carlos Eduardo Steiner Maria Letícia Cintra Antonia Paula Marques-de-Faria

We report on a 22-year-old male patient and his father, both presenting with congenital sensorineural deafness, diffuse palmoplantar keratoderma and knuckle pads. These findings are similar to those previously described in the Bart-Pumphrey syndrome, a rare autosomal dominant disorder. Several conditions including keratoderma and deafness are briefly reviewed.

2016
Sunil K Kothiwala Mahesh Prajapat CM Kuldeep

Christ-Siemens-Touraine syndrome is a form of anhidrotic ectodermal dysplasia (ED) characterized by triad of hypodontia, hypotrichosis, and hypohidrosis. Palmoplantar keratoderma is a characteristic feature of hidrotic forms of ED. Till date, only two cases have been reported of Christ-Siemens-Touraine syndrome with palmoplantar keratoderma; here we report a similar case emphasizing this rare a...

2014
V. Sindhuri Reddy M. Madhavi Latha

Pachyonychia congenita type II is an autosomal dominant inherited rare genodermatosis characterized by dystrophic wedge shaped thickened nails with subungual hyperkeratosis, symmetric palmoplantar keratoderma, steatocystoma multiplex. Here we report a 23-year-old male with characteristic features of dystrophic nails, palmoplantar keratoderma, steatocystoma multiplex, follicular hyperkeratotic p...

A Naser Tork AH Ehsani S Kavusi S Toosi

Mal de meleda (Keratoderma plamoplantaris transgrediens) is a rare autosomal recessive form of palmoplantar keratoderma with hyperkeratosis of palms and soles, which appears soon after birth and progressively involves other areas (Transgrediens) of the skin especially dorsal aspects of hands and feet. We report a 20-year-old woman with mal de meleda with some unusual clinical features, i....

Journal: :Dermatology Online Journal 2013

Journal: :BMJ case reports 2017
Ilda Coelho Sara Costa Sofia Silva Mendes Guilherme Castro Gomes

Coelho I, et al. BMJ Case Rep 2017. doi:10.1136/bcr-2017-222475 Description A 26-year-old woman, previously healthy, that a month ago started complaining of pain in the soles of both feet, which followed, additionally, to the right knee, the left knee, left elbow and right shoulder. She reported morning stiffness exceeding 1 hour that decreased with physical activity, worsened with rest, but im...

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