Constitutional trisomy 8 mosaicism due to meiosis II non-disjunction in a phenotypically normal woman with hematologic abnormalities

被引:14
作者
Baidas, S
Chen, TJ
Kolev, V
Wong, LJ
Imholte, J
Qin, NG
Meck, J
机构
[1] Georgetown Univ Hosp, Dept Med & Oncol, Washington, DC USA
[2] Georgetown Univ, Ctr Med, Inst Mol & Human Genet, Washington, DC USA
[3] Univ S Alabama, Dept Med Genet, Mobile, AL 36688 USA
关键词
trisomy; 8; mosaicism; meiosis II non-disjunction; Behcet's disease;
D O I
10.1002/ajmg.a.20390
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Constitutional trisomy 8 mosaicism (CT8M) in liveborns is typically caused by mitotic non-disjunction and exhibits wide phenotypic variability. By contrast, CT8M due to meiotic errors usually results in miscarriage. We describe a case of CT8M due to a paternal meiosis II non-disjunction error. The patient, a 32-year-old woman, was phenotypically normal except for a history of recurrent aphthous ulcers since childhood and a 4-year history of macrocytosis. The ulcers were refractory to steroids, but responded well to thalidomide. To the best of our knowledge, this is the first report of CT8M due to meiotic non-disjunction in a phenotypically normal individual. (C) 2003 Wiley-Liss, Inc.
引用
收藏
页码:383 / 387
页数:5
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