TUMORS IN RUBINSTEIN-TAYBI SYNDROME

被引:211
作者
MILLER, RW
RUBINSTEIN, JH
机构
[1] UNIV CINCINNATI,AFFILIATED CTR DEV DISORDERS,CINCINNATI,OH
[2] UNIV CINCINNATI,COLL MED,DEPT PEDIAT,CINCINNATI,OH
[3] CHILDRENS HOSP,MED CTR,CINCINNATI,OH 45229
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 1995年 / 56卷 / 01期
关键词
RUBINSTEIN-TAYBI SYNDROME; NEOPLASMS; BRAIN TUMORS; GERM CELL TUMORS; CONGENITAL ANOMALIES;
D O I
10.1002/ajmg.1320560125
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The 14 tumors reported in Rubinstein-Taybi syndrome since 1989, when added to the 22 previously reported, are beginning to show a pattern of neural and developmental tumors, especially of the head, which is malformed in the syndrome. Among the neoplasms were 12 of the nervous systems: 2 each of oligodendroglioma, medulloblastoma, neuroblastoma, and benign meningioma, a pheochromocytoma, and 3 other benign tumors; 2 of nasopharyngeal rhabdomyosarcoma; and 1 each of leiomyosarcoma, seminoma, and embryonal carcinoma. Among the other benign tumors were an odontoma, a choristoma, a dermoid cyst, and 2 pilomatrixomas. (C) 1995 Wiley-Liss, Inc.
引用
收藏
页码:112 / 115
页数:4
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