Neurocutaneous syndromes: neurofibromatosis 1, neurofibromatosis 2, and tuberous sclerosis

Curr Opin Neurol. 1997 Apr;10(2):131-6.

Abstract

Neurofibromatosis 1, neurofibromatosis 2, and tuberous sclerosis are a set of dominantly transmitted disorders that have in common the tendency towards formation of tumors of the nervous system and other tissues. The genes for neurofibromatosis 1, neurofibromatosis 2, and one of two forms of tuberous sclerosis have been identified and appear to act as tumor suppressor genes. Information is accumulating about pathogenesis that may eventually improve our ability to diagnose and treat these disorders.

Publication types

  • Review

MeSH terms

  • Child
  • Gene Expression Regulation, Neoplastic / physiology
  • Genes, Dominant / genetics
  • Genes, Tumor Suppressor / genetics
  • Humans
  • Molecular Biology
  • Neurofibromatosis 1 / diagnosis
  • Neurofibromatosis 1 / genetics*
  • Neurofibromatosis 2 / diagnosis
  • Neurofibromatosis 2 / genetics*
  • Tuberous Sclerosis / diagnosis
  • Tuberous Sclerosis / genetics*