Familial brain tumour syndrome associated with a p53 germline deletion of codon 236

Détails

ID Serval
serval:BIB_67641A583482
Type
Article: article d'un périodique ou d'un magazine.
Sous-type
Etude de cas (case report): rapporte une observation et la commente brièvement.
Collection
Publications
Institution
Titre
Familial brain tumour syndrome associated with a p53 germline deletion of codon 236
Périodique
Brain Pathology
Auteur⸱e⸱s
Lubbe  J., von Ammon  K., Watanabe  K., Hegi  M. E., Kleihues  P.
ISSN
1015-6305 (Print)
Statut éditorial
Publié
Date de publication
01/1995
Volume
5
Numéro
1
Pages
15-23
Notes
Case Reports
Journal Article
Research Support, Non-U.S. Gov't --- Old month value: Jan
Résumé
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.
Mots-clé
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
Création de la notice
25/01/2008 14:06
Dernière modification de la notice
20/08/2019 15:22
Données d'usage