PTEN hamartoma tumour syndrome: variability of an entity

J Med Genet. 2003 Oct;40(10):e111. doi: 10.1136/jmg.40.10.e111.
No abstract available

Publication types

  • Case Reports
  • Letter
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Child
  • Female
  • Germ-Line Mutation
  • Hamartoma Syndrome, Multiple / diagnosis*
  • Hamartoma Syndrome, Multiple / genetics*
  • Humans
  • Infant, Newborn
  • Male
  • PTEN Phosphohydrolase
  • Phenotype
  • Phosphoric Monoester Hydrolases / genetics*
  • Tomography, X-Ray Computed
  • Tumor Suppressor Proteins / genetics*

Substances

  • Tumor Suppressor Proteins
  • Phosphoric Monoester Hydrolases
  • PTEN Phosphohydrolase
  • PTEN protein, human

Associated data

  • OMIM/153480
  • OMIM/158350
  • OMIM/163200
  • OMIM/176920