Literature DB >> 15708285

Palmoplantar keratodermas.

Peter H Itin1, Susanna K Fistarol.   

Abstract

The palmoplantar skin is a highly specialized tissue which is able to resist mechanical trauma and other physical stress. In recent years the more descriptive classification of keratodermas has switched to an exact molecular genetic view where gene functions are considered. Palmoplantar keratodermas can be separated in the following functional subgroups: disturbed gene fuctions in structural proteins (keratins), cornified envelope (loricrin, transglutaminase), cohesion (plakophilin, desmoplakin, desmoglein1), cell-to-cell communication (connexins), and transmembrane signal transduction (cathepsin C). This review intends to emphasize the typical clinical aspects and symptom complexes associated with palmoplantar keratodermas which enable the astute dermatologist to make a clinical diagnosis. In addition the molecular genetic knowledge on the topic is given which is necessary to confirm the clinical diagnosis.

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Year:  2005        PMID: 15708285     DOI: 10.1016/j.clindermatol.2004.09.005

Source DB:  PubMed          Journal:  Clin Dermatol        ISSN: 0738-081X            Impact factor:   3.541


  19 in total

1.  [Keratosis palmoplantaris papulosa].

Authors:  C Mühlhoff; M Megahed
Journal:  Hautarzt       Date:  2012-05       Impact factor: 0.751

2.  Striate palmoplantar keratoderma resulting from a missense mutation in DSG1.

Authors:  D Vodo; E A O'Toole; N Malchin; A Lahav; N Adir; O Sarig; K J Green; F J D Smith; E Sprecher
Journal:  Br J Dermatol       Date:  2018-05-05       Impact factor: 9.302

3.  Lack of plakoglobin in epidermis leads to keratoderma.

Authors:  Deqiang Li; Wenjun Zhang; Ying Liu; Laura S Haneline; Weinian Shou
Journal:  J Biol Chem       Date:  2012-02-07       Impact factor: 5.157

Review 4.  Cytoglobin: biochemical, functional and clinical perspective of the newest member of the globin family.

Authors:  Urszula Oleksiewicz; Triantafillos Liloglou; John K Field; George Xinarianos
Journal:  Cell Mol Life Sci       Date:  2011-07-09       Impact factor: 9.261

Review 5.  Keratin gene mutations in disorders of human skin and its appendages.

Authors:  Jean Christopher Chamcheu; Imtiaz A Siddiqui; Deeba N Syed; Vaqar M Adhami; Mirjana Liovic; Hasan Mukhtar
Journal:  Arch Biochem Biophys       Date:  2010-12-19       Impact factor: 4.013

6.  Gene expression profiling in pachyonychia congenita skin.

Authors:  Yu-An Cao; Robyn P Hickerson; Brandon L Seegmiller; Dmitry Grapov; Maren M Gross; Marc R Bessette; Brett S Phinney; Manuel A Flores; Tycho J Speaker; Annaleen Vermeulen; Albert A Bravo; Anna L Bruckner; Leonard M Milstone; Mary E Schwartz; Robert H Rice; Roger L Kaspar
Journal:  J Dermatol Sci       Date:  2015-01-14       Impact factor: 4.563

7.  Autoimmune thyroiditis presenting as palmoplantar keratoderma.

Authors:  Sara Lestre; Eva Lozano; Cláudia Meireles; Ana Barata Feio
Journal:  Case Rep Med       Date:  2010-03-14

Review 8.  [Palmoplantar dermatoses: when should genes be considered?].

Authors:  C Seebode; S Schiller; S Emmert; K Giehl
Journal:  Hautarzt       Date:  2014-06       Impact factor: 0.751

Review 9.  The molecular basis of human keratin disorders.

Authors:  Meral Julia Arin
Journal:  Hum Genet       Date:  2009-02-27       Impact factor: 4.132

10.  Mutations in AQP5, encoding a water-channel protein, cause autosomal-dominant diffuse nonepidermolytic palmoplantar keratoderma.

Authors:  Diana C Blaydon; Lisbet K Lind; Vincent Plagnol; Kenneth J Linton; Francis J D Smith; Neil J Wilson; W H Irwin McLean; Colin S Munro; Andrew P South; Irene M Leigh; Edel A O'Toole; Anita Lundström; David P Kelsell
Journal:  Am J Hum Genet       Date:  2013-07-03       Impact factor: 11.025

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