Results 91 to 100 of about 1,347 (192)

Hereditary Painful Callosities Treated with L5 and S1 Pulsed Radiofrequency, Case Report

International Journal of Pain
Hereditary palmoplantar Keratoderma (PPK) varies in presentation, where palm and sole lesions can be diffuse, focal or punctate. There is no specific curative treatment for hereditary PPK, and the resulting pain may significantly strain all aspects of ...
Moustafa Moustafa, Kenneth Kuan Boon Keat, Hari Gopal   +2 more
doaj   +1 more source

Diffuse palmoplantar keratoderma associated with acrocyanosis. A family study.

Acta dermato-venereologica, 1989
Four members of a family, in which 8 suffered from diffuse palmoplantar keratoderma associated with an uncommon form of acrocyanosis, are reported. Acrocyanosis and palmoplantar keratoderma do not always occur together and, therefore, an autosomal dominant inheritance for this association is suggested.
openaire   +1 more source

QUERATODERMIA PALMOPLANTAR EPIDERMOLÍTICA (TIPO VÖRNER) - CARACTERIZAÇÃO DE UMA FAMÍLIA E REVISÃO DA LITERATURA

, 2014
Epidermolytic palmoplantar keratoderma (Vörner’s keratoderma) is an autosomal dominant disorder of keratinization characterized by diffuse, non-transgredient thickening of palms and soles, without associated ectodermal features.
Vieira, Fortunato, Peralta, Lígia, Matos, José, Morais, Paulo   +3 more
core   +1 more source

Cutaneous manifestations of hypothyroidism: An observational study in a tertiary care center of Eastern India

Asian Journal of Medical Sciences
Background: Changes in skin, hair, and nails may be initial manifestations of an underlying thyroid hormone deficiency. Symptomatic treatment of cutaneous manifestations without treatment of underlying hypothyroidism contributes to long-term morbidity in
Swastika Debbarma , Aniruddha Ghosh
doaj   +1 more source

Alitretinoin: A new treatment option for hereditary punctate palmoplantar keratoderma (Brauer-Buschke-Fischer syndrome)

, 2014
To the Editor: Punctate palmoplantar keratoderma type I (Brauer-Buschke-Fischer syndrome or PPKP1) is one of a group of heterogeneous disorders characterized by abnormal keratinization of the palms and soles.
Roberta Raboni, Raone, Beatrice, Patrizi, Annalisa, Raboni, Roberta   +3 more
core   +1 more source

Unna Thost Keratoderma palmoplantar . A Case Report

, 2011
The case of a 37 years old, black skinned, male patient who attended Dermatology Consultation in his health area is presented. The patient had skin lesions on the palms of his hands and the soles of his feet.
María Teresa Rodríguez Gandulla, Niurka Ramos Viera, Graciela Caridad Cabrera Acea   +2 more
core  

Case Report - Greither's disease

, 2004
A 14-year-old girl with diffuse palmoplantar keratoderma with hyperhidrosis and progressive extension of keratoderma to the dorsum of the hands and feet is reported.
S.B. Athanikar ,Arun C. Inamadar , Aparna Palit, V.V. Sampagavi , N.S. Deshmukh
core  

Additional file 1: of The first Danish family reported with an AQP5 mutation presenting diffuse non-epidermolytic palmoplantar keratoderma of Bothnian type, hyperhidrosis and frequent Corynebacterium infections: a case report

, 2016
Figure S1. Genetic test results of the proband. Bidirectional Sanger sequencing of the AQP5 gene. (PDF 617 kb)
Krøigård, Anne, Hetland, Liv, Clemmensen, Ole, Blaydon, Diana, Hertz, Jens, Bygum, Anette   +5 more
openaire   +1 more source

Diffuse palmoplantar keratoderma with painful fissures [PDF]

, 2020
openaire   +1 more source

Palmoplantaire keratodermie type Nagashima

, 2017
We describe a 15 year old patient diagnosed with Nagashima-type palmoplantar keratoderma (NPPK). NPPK is an autosomal recessive nonsyndromic diffuse palmoplantar keratosis mainly found in Japanese and Chinese populations.
Steijlen, P.M., van Geel, M., Ramakers, N.A.M., Vreeburg, Maaike   +3 more
core