نتایج جستجو برای: palmoplantar keratodermas

تعداد نتایج: 1515  

2014
Michaela Drögemüller Vidhya Jagannathan Doreen Becker Cord Drögemüller Claude Schelling Jocelyn Plassais Cécile Kaerle Caroline Dufaure de Citres Anne Thomas Eliane J. Müller Monika M. Welle Petra Roosje Tosso Leeb

Hereditary footpad hyperkeratosis (HFH) represents a palmoplantar hyperkeratosis, which is inherited as a monogenic autosomal recessive trait in several dog breeds, such as e.g. Kromfohrländer and Irish Terriers. We performed genome-wide association studies (GWAS) in both breeds. In Kromfohrländer we obtained a single strong association signal on chromosome 5 (p(raw) = 1.0×10(-13)) using 13 HFH...

2015
Ali Baykan Şeref Olgar Mustafa Argun Abdullah Özyurt Özge Pamukçu Kazım Üzüm Nazmi Narin

OBJECTIVE Naxos disease is an autosomal recessive, inherited, cardiocutaneous disorder, characterized by arrhythmogenic right ventricular cardiomyopathy, woolly hair, and palmoplantar keratoderma. Carvajal syndrome is characterized by palmoplantar keratoderma, curly hair, dilated cardiomyopathy, especially on the left ventricle side, and early morbidity. The aim of this study was to evaluate th...

Journal: :Actas Dermo-Sifiliográficas (English Edition) 2009

Journal: :QJM: An International Journal of Medicine 2018

Journal: :Nihon Shishubyo Gakkai Kaishi (Journal of the Japanese Society of Periodontology) 2018

2017
Thiviyani Maruthappu Anissa Chikh Benjamin Fell Paul J. Delaney Matthew A. Brooke Clemence Levet Angela Moncada-Pazos Akemi Ishida-Yamamoto Diana Blaydon Ahmad Waseem Irene M. Leigh Matthew Freeman David P. Kelsell

Keratin 16 (K16) is a cytoskeletal scaffolding protein highly expressed at pressure-bearing sites of the mammalian footpad. It can be induced in hyperproliferative states such as wound healing, inflammation and cancer. Here we show that the inactive rhomboid protease RHBDF2 (iRHOM2) regulates thickening of the footpad epidermis through its interaction with K16. K16 expression is absent in the t...

2018
Ji Young Choi Song Ee Kim Sang Eun Lee Soo Chan Kim

Olmsted syndrome (OS) is a rare congenital skin disorder characterized by severe palmoplantar and periorificial keratoderma, alopecia, onychodystrophy, and severe pruritus. Recently, pathogenic 'gain-of-function' mutations of the transient receptor potential vanilloid 3 gene (TRPV3), which encodes a cation channel involved in keratinocyte differentiation and proliferation, hair growth, inflamma...

Journal: :Dermatology online journal 2016
Megan E Prouty Ryan Fischer Deede Liu

Hyperhidrosis, or abnormally increased sweating, is a condition that may have a primary or secondary cause. Usually medication- induced secondary hyperhidrosis manifests with generalized, rather than focal sweating. We report a 32-year-old woman with a history of palmoplantar hyperhidrosis for 15 years who presented for treatment and was prescribed oral glycopyrrolate. One month later, the palm...

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