Literature DB >> 2699660

Ependymomas in two sisters and a maternal male cousin with mosaicism with monosomy 22 in tumour.

M L Savard1, D M Gilchrist.   

Abstract

A family with two sisters and their mother's male cousin had ependymomas. Of note is the fact that chromosome analysis on the tumour of the younger sister showed two cell lines, one a normal female line, the other with monosomy of chromosome 22.

Entities:  

Mesh：

Year:  1989        PMID： 2699660     DOI： 10.1159/000120447

Source DB:  PubMed          Journal:  Pediatr Neurosci        ISSN： 0255-7975


  3 in total

Review 1.  Uncommon pediatric tumors of the posterior fossa: pathologic and molecular features.

Authors:  C Dunham
Journal:  Childs Nerv Syst       Date:  2015-09-09       Impact factor: 1.475

2.  Familial anaplastic ependymoma: evidence of loss of chromosome 22 in tumour cells.

Authors:  P C Nijssen; R H Deprez; C C Tijssen; A Hagemeijer; E P Arnoldus; J L Teepen; R Holl; M F Niermeyer
Journal:  J Neurol Neurosurg Psychiatry       Date:  1994-10       Impact factor: 10.154

3.  Evidence for an ependymoma tumour suppressor gene in chromosome region 22pter-22q11.2.

Authors:  T J Hulsebos; N T Oskam; E H Bijleveld; A Westerveld; M A Hermsen; A M van den Ouweland; B C Hamel; C C Tijssen
Journal:  Br J Cancer       Date:  1999-12       Impact factor: 7.640
  3 in total

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