PTEN mutation in a Japanese boy with autonomously functioning thyroid nodule

Pediatr Int. 2017 Nov;59(11):1223-1224. doi: 10.1111/ped.13427.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Adenocarcinoma, Follicular / etiology*
  • Child, Preschool
  • Genetic Markers
  • Hamartoma Syndrome, Multiple / complications
  • Hamartoma Syndrome, Multiple / diagnosis*
  • Hamartoma Syndrome, Multiple / genetics
  • Humans
  • Japan
  • Male
  • Mutation, Missense*
  • PTEN Phosphohydrolase / genetics*
  • Thyroid Neoplasms / etiology*

Substances

  • Genetic Markers
  • PTEN Phosphohydrolase
  • PTEN protein, human