Hereditary Tumor Syndromes of the Nervous System: Overview and Rare Syndromes
- 1 April 1995
- journal article
- review article
- Published by Wiley in Brain Pathology
- Vol. 5 (2) , 145-151
- https://doi.org/10.1111/j.1750-3639.1995.tb00588.x
Abstract
Hereditary tumor syndromes of the nervous system are a varied group of conditions that include neurofibromatosis 1, neurofibromatosis 2, tuberous sclerosis, and von Hippel‐Lindau disease, as well as the retinoblastoma susceptibility, Li‐Fraumeni, familial glioma, Turcot, Gorlin, Cowden and multiple endocrine neoplasia syndromes. For many of these conditions, the responsible genes have been localized or identified. Such studies have elucidated the genetic basis of both hereditary cancer predisposition and sporadic nervous system tumors. The first four hereditary tumor syndromes have been extensively studied and are discussed in detail in the four subsequent articles. The other syndromes have also been subject to both pathological and molecular genetic inquiries. In this introductory overview, we discuss the features common to the hereditary tumor syndromes of the nervous system, and review some of the rarer conditions.Keywords
This publication has 47 references indexed in Scilit:
- The Multiple Tumor Suppressor 1/Cyclin-dependent Kinase Inhibitor 2 Gene in Human Central Nervous System Primitive Neuroectodermal TumorNeurosurgery, 1995
- Glioblastoma multiforme in four siblings: A cytogenetic and molecular genetic studyJournal of Neuro-Oncology, 1995
- Dynamic mutations hit double figuresNature Genetics, 1994
- Association of Lhermitte-Duclos and Cowden disease: report of a new case and review of the literature.Journal of Neurology, Neurosurgery & Psychiatry, 1994
- Absence of hereditary mutations in exons 5 through 9 of the p53 gene and exon 24 of the neurofibromin gene in families with gliomaAnnals of Neurology, 1994
- Cowden syndrome: report of a large family with macrocephaly and increased severity of signs in subsequent generationsClinical Genetics, 1993
- Genetic evidence that Turcot syndrome is not allelic to familial adenomatous polyposisAmerican Journal of Medical Genetics, 1992
- Neurocutaneous melanosis: Definition and review of the literatureJournal of the American Academy of Dermatology, 1991
- Brain tumours and the occurrence of severe invasive basal cell carcinoma in first degree relatives with Gorlin syndromeBritish Journal Of Neurosurgery, 1991
- Mutation and Cancer: Statistical Study of RetinoblastomaProceedings of the National Academy of Sciences, 1971