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Objective  Mutations in  CD59  cause CIDP-like polyneuropathy in children with inherited chronic hemolysis. We hypothesized that mutations in  CD59  might be found in a subset of sporadic CIDP patients.    Methods  35 patients from two centers, fulfilling the EFNS/PNS diagnostic criteria for CIDP were included.  CD59  coding region was amplified by PCR and Sanger sequenced.    Results  One rare variant was detected in a patient which resulted in a synonymous change and predicted to be neutral. Pathogenic variants were absent in our cohort.    Interpretation  Our pilot study suggests that mutations in  CD59  are absent in adult-onset sporadic CIDP.

Absence of pathogenic mutations in CD59 in chronic inflammatory demyelinating polyradiculoneuropathy