A 163-bp deletion in the neurofibromatosis 2 (NF2) gene associated with variant phenotypes [corrected]

Hum Genet. 1995 Apr;95(4):443-6. doi: 10.1007/BF00208973.

Abstract

We have analyzed cDNA from a 46-year-old atypical neurofibromatosis type 2 (NF2) patient who had lumbar tumors, cataract and schwannomas of peripheral nerves but no vestibular schwannomas, and have identified a 163-bp deletion in the NF2 transcript. The deletion is predicted to remove 54, alter 15 and add four extra amino acids at the C-terminus of the NF2-gene product. The same deletion was found in her two daughters and in a 3-year-old grandson. Bilateral vestibular schwannomas were detected in the two asymptomatic daughters, whereas no abnormality was found in the grandson.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Cataract / genetics
  • Child, Preschool
  • DNA Mutational Analysis
  • DNA, Neoplasm / analysis*
  • Female
  • Gene Deletion*
  • Genes, Neurofibromatosis 2 / genetics*
  • Genotype
  • Humans
  • Male
  • Middle Aged
  • Neurilemmoma / genetics*
  • Neurofibromatosis 2 / genetics*
  • Pedigree
  • Phenotype
  • Spinal Cord Neoplasms / genetics*

Substances

  • DNA, Neoplasm