Medulloblastoma in a child with Rubenstein-Taybi Syndrome: Case report and review of the literature

被引:18
|
作者
Taylor, MD [1 ]
Mainprize, TG [1 ]
Rutka, JT [1 ]
Becker, L [1 ]
Bayani, J [1 ]
Drake, JM [1 ]
机构
[1] Hosp Sick Children, Toronto, ON M5G 1X8, Canada
关键词
medulloblastoma; Rubenstein-Taybi syndrome; familial cancer; genetics; CBP gene; hereditary neoplasm;
D O I
10.1159/000050428
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
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 (C) 2001 S. Karger AG, Basel.
引用
收藏
页码:235 / 238
页数:4
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