Objective Morvan syndrome is characterized by central, autonomic, and peripheral hyperexcitability due to contactin-associated protein 2 (CASPR2) antibody. Our objective …
SJ Zhang, YY Xue, H Yu, QQ Tao - BMC neurology, 2021 - Springer
Abstract Background Morvan syndrome (MoS) is a rare autoimmune syndrome associated with antibodies against two kinds of potassium channel proteins, contactin associated …
M Benucci, L Tramacere, M Infantino… - Case Reports in …, 2020 - Wiley Online Library
We report the case of a 64‐year‐old man who presented with subacute memory, balance impairment, behavioral and mood changes, and epileptic seizures. Magnetic resonance …
W Masood, F Lui, KK Sitammagari - StatPearls [Internet], 2024 - ncbi.nlm.nih.gov
Objectives: Identify the signs and symptoms of Morvan syndrome. Interpret antibody testing results and plan treatment accordingly. Select a treatment modality that best suits the clinical …
O Sveinsson, F Al Nimer, F Piehl - BMJ Case Reports CP, 2019 - casereports.bmj.com
We describe a woman with both central and peripheral nervous system symptoms consistent with Morvan's syndrome who was successfully treated with immunosuppression including …
B Eikeland - Case Reports in Neurological Medicine, 2020 - Wiley Online Library
Research in the last few years has indicated that most voltage‐gated potassium channel‐ (VGKC‐) complex antibodies without leucine‐rich glioma‐inactivated protein 1 or contactin …
S Alagoda, S Wimalaratna… - BMJ Case Reports CP, 2023 - casereports.bmj.com
A man in his mid-60s presented with a 3-month history of progressive muscle twitching, agitation, cognitive impairment, insomnia, hyperhidrosis and lower limb pain. He had …
DM Sindhu, S Rao, A Mahadevan, M Netravathi - Neurology India, 2024 - journals.lww.com
Morvan's syndrome is a rare, complex autoimmune syndrome comprising peripheral nerve hyperexcitability, dysautonomia, insomnia, and encephalopathy. In this case report, we …
D Park, J Means, AW Campion… - American Journal of …, 2024 - search.ebscohost.com
Abstract Objective: Rare disease Background: Morvan fibrillary chorea (Morvan syndrome) is a rare disorder marked by a collection of neurological symptoms such as myokymia …