Hepatolenticular Degeneration Combined with Primary Antiphospholipid Syndrome: A Case Report

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Hepatolenticular degeneration combined with primary antiphospholipid syndrome: a case report.

biochemical parameters were within the normal reference ranges. Thrombocytes were 77 ! 10 9 /l; neither thrombocyte aggregation nor schistocytes were found on peripheral blood smear examination. The autoantibodies against ds-DNA, Sm, Ro/ SS-A, La/SS-B and RNP antigens (ELISA) and ANA titer (1: 40 HEP-2) were negative. The antiphospholipid antibodies – IgG isotype (48 GPL) and IgM isotype (56 GP...

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Hepatolenticular Degeneration (Wilson's Disease)

A R?eport of five cases, with Commentary WILSON'S disease is a heredo-familial disorder, the essential pathological elements of which consist in a cirrhotic state of the liver comb;ned with degenerative changes in the lenticular nuclei of the brain. The term "hepatolenticular degenera-tion" is therefore aptly precise, but affords little clue to the diversity of the clinical manifestations. A lo...

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ژورنال

عنوان ژورنال: European Neurology

سال: 2006

ISSN: 0014-3022,1421-9913

DOI: 10.1159/000091426