Cookies on this website

We use cookies to ensure that we give you the best experience on our website. If you click 'Accept all cookies' we'll assume that you are happy to receive all cookies and you won't see this message again. If you click 'Reject all non-essential cookies' only necessary cookies providing core functionality such as security, network management, and accessibility will be enabled. Click 'Find out more' for information on how to change your cookie settings.

Morvan's syndrome is a rare disease characterized by peripheral nerve hyperexcitability, associated with CNS and autonomic systems involvement. High serum voltage-gated potassium channel (VGKC) antibody titers have been reported, and, till now, Morvan's syndrome has been considered as a VGKC antibody associated disease. We describe a patient with Morvan's syndrome associated with myasthenia gravis and a thymoma in his previous history, with surprisingly undetectable levels of VGKC antibodies. The clinical course is similar to those cases of Morvan's syndrome with VGKC-Ab, except for the lack of response to plasma exchange, previously considered as the first choice treatment. Nevertheless, the good response to corticosteroids therapy and the association with myasthenia confirm an autoimmune origin of the disease.

Original publication

DOI

10.1007/s10072-009-0041-y

Type

Journal article

Journal

Neurol Sci

Publication Date

06/2009

Volume

30

Pages

237 - 239

Keywords

Adrenal Cortex Hormones, Autoantibodies, Humans, Male, Middle Aged, Myasthenia Gravis, Myokymia, Plasma Exchange, Potassium Channels, Voltage-Gated, Prednisone, Ryanodine Receptor Calcium Release Channel, Treatment Outcome