| Literature DB >> 7931388 |
P C Nijssen1, R H Deprez, C C Tijssen, A Hagemeijer, E P Arnoldus, J L Teepen, R Holl, M F Niermeyer.
Abstract
A family with anaplastic ependymomas, histologically verified in three cases and neuroradiologically suggested in a fourth, is presented. Two healthy brothers both had two affected sons. All four male patients were younger than 5 years at the time of diagnosis. Two boys died before the age of 3 years. Genotype analysis (with polymorphic DNA markers for chromosome 22 and interphase cytogenetic analysis) of one of the tumours showed a subpopulation of tumour cells with monosomy of (part of) chromosome 22. Non-neoplastic cells of this patient showed a normal karyotype. These findings give further evidence for the role of a tumour suppressor gene on chromosome 22 in the pathogenesis of familial ependymal tumours.Entities:
Mesh:
Year: 1994 PMID: 7931388 PMCID: PMC485495 DOI: 10.1136/jnnp.57.10.1245
Source DB: PubMed Journal: J Neurol Neurosurg Psychiatry ISSN: 0022-3050 Impact factor: 10.154