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Acral keratosis

Known as: Acral keratoses 
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
Cowden syndrome (CS) is a rare autosomal dominant, hereditary, multiorgan disease with higher risk for malignancies (breast… 
2017
2017
Cowden syndrome (CS) is an uncommon autosomal dominant multiorgan/system genodermatosis. It is characterized by the development… 
2015
2015
Here, we report a case of Cowden syndrome with an unusual clinical course of late-onset oral papillomatosis and a novel germline… 
2012
2012
Cowden syndrome is a rare genodermatosis characterized by the formation of hamartomas in various organs and increased risk of… 
2008
2008
TO THE EDITOR: In the article by Lu et al, 1 the investigators conducted a prospective assessment of the prevalence of Lynch… 
2006
2006
Cowden disease (CD) is a rare autosomal dominant disease with variable expression, affecting a number of systems in the form of… 
Review
2004
Review
2004
  • J. Reifenberger
  • 2004
  • Corpus ID: 6948519
Several hereditary tumor syndromes are associated with characteristic skin lesions which may facilitate an early diagnosis. We… 
2004
2004
ZusammenfassungEine Reihe von hereditären Tumorsyndromen zeichnet sich durch charakteristische Veränderungen der Haut aus, die… 
1987
1987
REPORT OF A CASE A 62-year-old man had thyroid goiter (Fig 1) of approximately ten years' duration. There were no signs or…