Skip to search formSkip to main contentSkip to account menu

PALMOPLANTAR KERATODERMA, NONEPIDERMOLYTIC

Known as: Nonepidermolytic palmoplantar keratoderma, NEPPK, KERATODERMA, NONEPIDERMOLYTIC PALMOPLANTAR 
National Institutes of Health

Related topics

Related topics

5 relations
Autosomal dominant inheritanceHyperkeratosisKRT16 geneKeratoderma, Palmoplantar, Epidermolytic

Broader (1)

Keratoderma, Palmoplantar, Diffuse

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
Novel Splice-Site Mutation of KRT1 Underlies Diffuse Palmoplantar Keratoderma in a Large Chinese Pedigree.
AIMS To identify potential causative gene mutations in a large Han Chinese pedigree with diffuse nonepidermolytic palmoplantar… 
2005
2005
A7445G mtDNA mutation present in a Portuguese family exhibiting hereditary deafness and palmoplantar keratoderma
Mitochondrial DNA (mtDNA) A7445G point mutation has been shown to be responsible for familial nonepidermolytic palmoplantar… 
2001
2001
Novel keratin 17 mutations in pachyonychia congenita type 2.
Pachyonychia congenita type 2 is an inherited ectodermal dysplasia characterized by hypertrophic nail dystrophy and multiple… 
1999
1999
Envoplakin, a possible candidate gene for focal NEPPK/esophageal cancer (TOC): the integration of genetic and physical maps of the TOC region on 17q25.
Focal nonepidermolytic palmoplantar keratoderma (NEPPK), or tylosis, is an autosomal, dominantly inherited disorder of the skin… 
By clicking accept or continuing to use the site, you agree to the terms outlined in our Privacy Policy (opens in a new tab), Terms of Service (opens in a new tab), and Dataset License (opens in a new tab)