| Literature DB >> 11741116 |
M D Taylor1, T G Mainprize, J T Rutka, L Becker, J Bayani, J M Drake.
Abstract
Although medulloblastoma is usually sporadic, there are a number of uncommon predisposing germline mutation syndromes, including: Gorlin's Syndrome, Turcot's Syndrome and Li-Fraumeni Syndrome. Patients with Rubenstein-Taybi Syndrome secondary to mutation/deletion of the CBP gene on chromosome 16 are predisposed to a variety of developmental anomalies as well as cancer. We report a child with Rubenstein-Taybi syndrome who developed a cerebellar medulloblastoma and review the literature on Rubenstein-Taybi Syndrome and pediatric medulloblastoma. As the product of the CBP gene functions in a variety of signaling pathways, we discuss the molecular implications of findings a medulloblastoma in a child with Rubenstein-Taybi Syndrome. Copyright 2001 S. Karger AG, BaselEntities:
Mesh:
Year: 2001 PMID: 11741116 DOI: 10.1159/000050428
Source DB: PubMed Journal: Pediatr Neurosurg ISSN: 1016-2291 Impact factor: 1.162