Homozygous PTEN deletion in neuroblastoma arising in a child with Cowden syndrome

Am J Med Genet A. 2011 Jul;155A(7):1763-6. doi: 10.1002/ajmg.a.34066. Epub 2011 Jun 10.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Child, Preschool
  • Chromosome Deletion
  • Chromosomes, Human, Pair 10 / genetics
  • Female
  • Gene Deletion*
  • Hamartoma Syndrome, Multiple / complications*
  • Hamartoma Syndrome, Multiple / genetics*
  • Homozygote*
  • Humans
  • Neuroblastoma / complications*
  • Neuroblastoma / genetics*
  • PTEN Phosphohydrolase / genetics*

Substances

  • PTEN Phosphohydrolase
  • PTEN protein, human

Supplementary concepts

  • Chromosome 10, monosomy 10q