After a century of study, mutations in connexin32, peripheral myelin protein22, and protein zero are now known to culminate in the prototypical phenotype of Charcot-Marie-Tooth disease. Many of these mutations have been modeled in rodents and in tissue culture. Consequently, structure-function predi
Peripheral neuropathy in cold agglutinin disease
✍ Scribed by MD T. Darrell Thomas; MD Peter D. Donofrio; MD Jean Angelo
- Publisher
- John Wiley and Sons
- Year
- 1991
- Tongue
- English
- Weight
- 339 KB
- Volume
- 14
- Category
- Article
- ISSN
- 0148-639X
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Cold agglutinin disease (CAD) characteristically presents as anemia and cold‐induced rash. We report a man with purpura, anemia, cold agglutinins, and a sensory‐autonomic polyneuropathy. Treatment with corticosteroids and plasma exchange resulted in resolution of the anemia and polyneuropathy. We propose that CAD may be associated with a reversible sensory‐autonomic neuropathy in the absence of cryoglobulinemia. Although unsupported by pathologic findings, pathogenetic hypotheses for the neuropathy in CAD are similar to those proposed for cryoglobulinemic neuropathy.
📜 SIMILAR VOLUMES