Chorea associated with antiphospholipid antibodies in a patient with Kabuki syndrome

被引:10
|
作者
Gidwani, Pooja
Segal, Eric
Shanske, Alan
Driscoll, Catherine
机构
[1] Childrens Hosp, Div Hematol Oncol, Bronx, NY 10467 USA
[2] Childrens Hosp, Ctr Craniofacial Disorders, Bronx, NY 10467 USA
关键词
Kabuki syndrome; chorea; anti-phospholipid antibodies; immune disorders;
D O I
10.1002/ajmg.a.31774
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Kabuki syndrome, OMIM 147920 (KS) is a disorder characterized by multi-system abnormalities. These include physical, neurological, endocrine, and autoimmune abnormalities. Multiple. autoimmune abnormalities are described in KS such as immune thrombocytopenic purpura (ITP), vitiligo, thyroiditis, hemolytic aneinia, and hypogammaglo-bulinemia. in this report, we describe a patient with KS with sudden onset chorea associated with the presence of antiphospholipid antibodies (aPLs) in the serum. Chorea in the presence of aPLs has been well described in the literature both in the presence and absence of antiphospholipid syndrome (APS) and systemic lupus erythematosus (SLE). This report of APT, in a patient with KS adds to the list of autoimmune disorders seen in patients with KS and also strengthens the hypothesis that patients with this syndrome have an increased incidence of immune dysregulation. (c) 2007 Wiley-Liss, Inc.
引用
收藏
页码:1338 / 1341
页数:4
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