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Als-Laus Syndrome in a Patient With High Level of Antiphospholipid Antibodies: A Case Report Pubmed



Saadatnia M1 ; Fatehi F2 ; Basiri K1 ; Sariaslani P1
Authors
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Authors Affiliations
  1. 1. Neurology Department, Isfahan Neurosciences Research Center, Isfahan University of Medical Sciences, Isfahan, Iran
  2. 2. Neurology Department, Isfahan Neurosciences Research Center and Medical Education Research Center, Isfahan University of Medical Sciences, Isfahan, Sofeh Street, Iran

Source: Neurologia i Neurochirurgia Polska Published:2008


Abstract

When evaluating a patient with amyotrophic lateral sclerosis (ALS), a number of other motor neuron disorders and related motor syndromes should be considered. Herein, we describe a 55-year-old Persian man with typical presentation of ALS in whom based on further finding of elevated level of antiphospholipid antibodies, final diagnosis of ALS with laboratory abnormalities of uncertain significance (ALS-LAUS) was made. With respect to persistent increased titre of antiphospholipid antibodies, he was treated with plasma exchange and prednisolone. After 3 months of treatment, the symptoms improved and antiphospholipid antibody titres decreased. To the best of our knowledge, this is the first case of ALS-LAUS accompanied by high titre of antiphospholipid antibodies with response to plasma exchange and corticosteroids.