Maternal germinal mosaicism of X-linked agammaglobulinemia

被引:0
作者
Sakamoto, M
Kanegane, H
Fujii, H
Tsukada, S
Miyawaki, T
Shinomiya, N
机构
[1] Toho Univ, Sch Med, Dept Pediat 2, Tokyo, Japan
[2] Toyama Med & Pharmaceut Univ, Fac Med, Dept Pediat, Toyama, Japan
[3] Osaka Univ, Sch Med, Dept Mol Med, Osaka, Japan
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 2001年 / 99卷 / 03期
关键词
X-linked agammaglobulinemia; BTK protein; BTK gene; germinal mosaicism;
D O I
10.1002/1096-8628(2001)9999:9999<::AID-AJMG1159>3.0.CO;2-M
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
X-linked agammaglobulinemia (XLA) is an immunodeficiency caused by abnormalities in tyrosine kinase (BTK), and is characterized by a deficiency of peripheral blood B cells. We studied cytoplasmic expression of BTK protein and analyzed the BTK gene (BTK) in peripheral blood mononuclear cells from two siblings with XLA and additional family members. Cytoplasmic expression of BTK protein in monocytes was not detected in either patient with XLA, A single base deletion (C563) in BTK-exon 6, which encodes the TH domain, was identified in both XLA patients. However, normal cytoplasmic expression of BTK protein in monocytes was detected in their mother without any BTK mutation, These results strongly suggest germinal mosaicism in the mother. (C) 2001 Wiley-Liss, Inc.
引用
收藏
页码:234 / 237
页数:4
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