EEC syndrome type 3 with a heterozygous germline mutation in the P63 gene and B cell lymphoma

被引:22
作者
Akahoshi, K
Sakazume, S
Kosaki, K
Ohashi, H
Fukushima, Y
机构
[1] Shimada Ryoiku Ctr, Dept Med Genet, Tokyo, Japan
[2] Shinshu Univ, Sch Med, Dept Med Genet, Matsumoto, Nagano 390, Japan
[3] Keio Univ, Sch Med, Dept Pediat, Tokyo, Japan
[4] Saitama Childrens Med Ctr, Dept Med Genet, Iwatsuki, Saitama, Japan
来源
AMERICAN JOURNAL OF MEDICAL GENETICS PART A | 2003年 / 120A卷 / 03期
关键词
EEC syndrome; p63; B-cell lymphoma; apoptosis;
D O I
10.1002/ajmg.a.20064
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Lines of evidence have recently indicated a relationship between mutations in the P63 gene and ectrodactyly-ectodermal dysplasia-clefting (EEC) syndrome type 3 (EEC3). The p63 gene (P63) has homology to P53 known as a tumor-suppressor gene, but biological function of its protein has not yet been known well. There have been two reported patients who had EEC syndrome associated with malignant lymphoma. However, they did not undergo sequencing analysis of P63. Here, we present with a Japanese girl who had EEC3 and developed diffuse large B-cell type non-Hodgkin lymphoma. In this patient, we documented a heterozygous germline mutation, Asp312Gly, in P63. We speculated that p63 may exert a biological function as a tumor suppressor. Malignant lymphoma should be considered as an important complication of EEC3. (C) 2003 Wiley-Liss, Inc.
引用
收藏
页码:370 / 373
页数:4
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