Familial brain tumour syndrome associated with a p53 germline deletion of codon 236
Details
Serval ID
serval:BIB_67641A583482
Type
Article: article from journal or magazin.
Publication sub-type
Case report (case report): feedback on an observation with a short commentary.
Collection
Publications
Institution
Title
Familial brain tumour syndrome associated with a p53 germline deletion of codon 236
Journal
Brain Pathology
ISSN
1015-6305 (Print)
Publication state
Published
Issued date
01/1995
Volume
5
Number
1
Pages
15-23
Notes
Case Reports
Journal Article
Research Support, Non-U.S. Gov't --- Old month value: Jan
Journal Article
Research Support, Non-U.S. Gov't --- Old month value: Jan
Abstract
This report describes clinical, neuropathological and molecular genetic findings in a Swiss family with four brain tumours in only two generations. The neoplasms observed covered a wide range of biologic behaviour, from a slowly growing lesion already apparent at birth, to anaplastic astrocytoma in a young adult and glioblastomas at the age of less than 10 years. The only non-neural neoplasms in this family were a case of leukemia and an adrenocortical carcinoma. A germline deletion of codon 236 of the p53 tumour suppressor gene was identified as an underlying cause and detected in all affected family members. This mutation has not previously been reported as germline transmission or in sporadic tumours. The unusual accumulation of CNS tumours may be due to a certain organ-specific effect of this particular p53 mutation or it may reflect the specific genetic back-ground of this family.
Keywords
Adult
Aged
Base Sequence
Brain Neoplasms/*genetics/pathology
Child
Child, Preschool
Codon
Female
*Genes, p53
*Germ-Line Mutation
Humans
Immunohistochemistry
Male
Molecular Sequence Data
Pedigree
Polymerase Chain Reaction
*Sequence Deletion
Pubmed
Web of science
Create date
25/01/2008 13:06
Last modification date
20/08/2019 14:22