[Cowden syndrome diagnosed in patients with macrocephaly]

Ugeskr Laeger. 2014 Jan 20;176(2):165-7.
[Article in Danish]

Abstract

Cowden syndrome is a rare autosomal dominant syndrome with a predisposition to cancer. We present a case of Cowden syndrome in a mother and her son, who were diagnosed with palmoplantar hyperkeratosis, macrocephaly and goitre. Early diagnosis is a challenge as the patients present with a variety of symptoms, but it is important because of the risk of cancer.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Cephalometry
  • Female
  • Genetic Predisposition to Disease
  • Goiter / diagnosis
  • Hamartoma Syndrome, Multiple / diagnosis*
  • Hamartoma Syndrome, Multiple / genetics
  • Hamartoma Syndrome, Multiple / pathology
  • Humans
  • Keratoderma, Palmoplantar / pathology
  • Male
  • Megalencephaly / diagnosis
  • Middle Aged
  • Mutation
  • PTEN Phosphohydrolase / genetics
  • Warts / diagnosis

Substances

  • PTEN Phosphohydrolase