FAMILIAL SNEDDON-SYNDROME - CLINICAL, HEMATOLOGIC, AND RADIOGRAPHIC FINDINGS IN 2 BROTHERS

被引:34
作者
PETTEE, AD
WASSERMAN, BA
ADAMS, NL
MCMULLEN, W
SMITH, HR
WOODS, SL
RATNOFF, OD
机构
[1] UNIV HOSP CLEVELAND,DEPT MACROMOLEC CHEM,CLEVELAND,OH 44106
[2] UNIV HOSP CLEVELAND,DEPT DERMATOL,CLEVELAND,OH 44106
[3] UNIV HOSP CLEVELAND,DIV RHEUMATOL,CLEVELAND,OH 44106
[4] UNIV HOSP CLEVELAND,DIV HEMATOL & ONCOL,CLEVELAND,OH 44106
[5] UNIV HOSP CLEVELAND,DEPT MED,CLEVELAND,OH 44106
[6] CASE WESTERN RESERVE UNIV,CLEVELAND,OH 44106
[7] VET ADM MED CTR,DEPT PSYCHOL,CLEVELAND,OH 44106
[8] VET ADM MED CTR,DIV RHEUMATOL,CLEVELAND,OH 44106
[9] VET ADM MED CTR,DEPT MED,CLEVELAND,OH 44106
关键词
D O I
10.1212/WNL.44.3_Part_1.399
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
We present the clinical, hematologic, and radiographic findings in two brothers with Sneddon's syndrome (stroke and livedo reticularis) and antiphospholipid antibodies. Patient 1 had anticardiolipin antibody and patient 2 had lupus anticoagulant, which we detected only upon repeated blood testing. One should test for both anticardiolipin antibody and lupus anticoagulant and repeat the screenings before determining a Sneddon's syndrome patient's antiphospholipid antibody status. Both Sneddon's syndrome and the primary antiphospholipid antibody syndrome are potentially familial causes of stroke. In familial cases, an inherited predisposition to antiphospholipid antibody production may be involved in disease pathogenesis.
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页码:399 / 405
页数:7
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