Willison, HJ and O'Leary, CP and Veitch, J and Blumhardt, LD and Busby, M and Donaghy, M and Fuhr, P and Ford, H and Hahn, A and Renaud, S and Katifi, HA and Ponsford, S and Reuber, M and Steck, A and Sutton, I and Schady, W and Thomas, PK and Thompson, AJ and Vallat, JM and Winer, J (2001) The clinical and laboratory features of chronic sensory ataxic neuropathy with anti-disialosyl IgM antibodies. BRAIN , 124 1968 - 1977.
Full text not available from this repository.
The clinical and laboratory phenotype of a paraproteinaemic neuropathy syndrome termed chronic sensory ataxic neuropathy with anti-disialosyl IgM antibodies is described in a series of 18 cases. Previous single case reports have outlined some features of this syndrome. All 18 cases were defined by the presence of serum IgM antibodies which react principally with NeuAc (alpha2-8)NeuAc(alpha2-3)Gal-configured disialosyl epitopes common to many gangliosides including GD1b, GD3, GT1b and GQ1b. In 17 out of 18 cases, the serum contained benign IgM paraproteins, and in four of these cases at least two IgM paraproteins were present. The IgM antibodies were also cold agglutinins in 50% of cases. The clinical picture comprised a chronic neuropathy with marked sensory ataxia and areflexia, and with relatively preserved motor function in the limbs. In addition, 16 out of 18 cases had motor weakness affecting oculomotor and bulbar muscles as fixed or as relapsing-remitting features. When present in their entirety, these clinical features have been described previously under the acronym CANOMAD: chronic ataxic neuropathy, ophthalmoplegia, IgM paraprotein, cold agglutinins and disialosyl antibodies. This distribution of clinical features is reminiscent of Miller Fisher syndrome, in which acute-phase anti-disialylated ganglioside IgG antibodies are found. Clinical electrophysiology and nerve biopsy show both demyelinating and axonal features. A partial response to intravenous immunoglobulin and other treatments is reported in some cases.
|Title:||The clinical and laboratory features of chronic sensory ataxic neuropathy with anti-disialosyl IgM antibodies|
|Keywords:||sensory ataxic neuropathy, CANOMAD, paraproteinaemia, disialosyl antibodies, Miller Fisher syndrome, MILLER-FISHER-SYNDROME, GUILLAIN-BARRE-SYNDROME, CAMPYLOBACTER-JEJUNI LIPOPOLYSACCHARIDES, HUMAN PERIPHERAL-NERVE, MONOCLONAL GAMMOPATHY, M-PROTEIN, ANTIGANGLIOSIDE ANTIBODIES, UNDETERMINED SIGNIFICANCE, ANTI-GQ1B ANTIBODIES, COLD AGGLUTININS|
|UCL classification:||UCL > School of Life and Medical Sciences > Faculty of Brain Sciences|
Archive Staff Only: edit this record