Clinical and positron emission tomography findings of chorea associated with primary antiphospholipid antibody syndrome
Identifieur interne : 001794 ( PascalFrancis/Curation ); précédent : 001793; suivant : 001795Clinical and positron emission tomography findings of chorea associated with primary antiphospholipid antibody syndrome
Auteurs : Steve W. Wu [États-Unis] ; Brent Graham [États-Unis] ; Michael J. Gelfand [États-Unis] ; Ralph E. Gruppo [États-Unis] ; Argirios Dinopolous [États-Unis] ; Donald L. Gilbert [États-Unis]Source :
- Movement disorders [ 0885-3185 ] ; 2007.
Descripteurs français
- Pascal (Inist)
English descriptors
- KwdEn :
Abstract
A fourteen-year-old right-handed male with a history of attention deficit hyperactivity disorder (ADHD) presented with alternating hemichorea. Laboratory findings included elevated anticardiolipin IgG and anti-β2-glycoprotein I IgG, which were consistent with primary antiphospholipid antibody syndrome. Positron emission tomography (PET) imaging revealed altered striatal metabolism in his left putamen while he was exhibiting right-sided hemichorea. His symptoms resolved on prednisone; however, his antiphospholipid antibody profile remained markedly abnormal despite being symptom-free for 26 months.
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<front><div type="abstract" xml:lang="en">A fourteen-year-old right-handed male with a history of attention deficit hyperactivity disorder (ADHD) presented with alternating hemichorea. Laboratory findings included elevated anticardiolipin IgG and anti-β<sub>2</sub>
-glycoprotein I IgG, which were consistent with primary antiphospholipid antibody syndrome. Positron emission tomography (PET) imaging revealed altered striatal metabolism in his left putamen while he was exhibiting right-sided hemichorea. His symptoms resolved on prednisone; however, his antiphospholipid antibody profile remained markedly abnormal despite being symptom-free for 26 months.</div>
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