Results 121 to 130 of about 1,153,947 (162)

Morvan Syndrome Following B-cell Lymphoma

open access: yesJournal of Child Neurology, 2010
Morvan syndrome is a rare autoimmune disease named after the French physician Augustin Marie Morvan. It is characterized by multiple, irregular contractions of the long muscles, weakness, pruritus, hyperhidrosis, insomnia, and delirium. Here, we describe a 17-year-old young man, previously diagnosed with B-cell lymphoma, who presented with multiple ...
Mohamad K, El-Bitar   +4 more
openaire   +3 more sources

Morvan's syndrome: Clinical, laboratory, and in vitro electrophysiological studies

Muscle and Nerve, 2004
AbstractMorvan's syndrome is a rare disorder characterized by neuromyotonia, hyperhidrosis, and central nervous system dysfunction. We report a patient with features of this syndrome, but who initially presented with breathing difficulties. Concentric needle electromyography showed an abundance of myokymic and neuromyotonic discharges.
Karlheinz Reiners   +2 more
exaly   +3 more sources

Neurophysiologic Studies in Morvan Syndrome

Journal of Clinical Neurophysiology, 2004
This study was conducted to clarify the clinical and neurophysiologic characteristics of patients with Morvan syndrome, and to compare and contrast this syndrome with other forms of autoimmune encephalitis. A retrospective chart review of the clinical features and neurophysiologic studies of two cases of Morvan syndrome seen at the Mayo Clinic was ...
Keith A, Josephs   +5 more
openaire   +2 more sources

Reduplicative paramnesia in Morvan's syndrome

Journal of the Neurological Sciences, 2008
Morvan's syndrome is characterized by peripheral nervous system hyperexcitibility (myokymia and neuromyotonia), hyperhydrosis, sleep disorder, limb paresthesias, and encephalopathy. Voltage gated potassium channel antibodies (VGKC abs) are frequently present.
Lynsee A, Hudson   +5 more
openaire   +2 more sources

Atypical case of Morvan’s syndrome

Journal of Clinical Neuroscience, 2016
Morvan's syndrome is a rare neurological condition characterized by the combination of neuromyotonia, autonomic instability and encephalopathy, associated with auto-antibodies against voltage-gated potassium channels. We report a patient with an initial presentation suggestive of typical Guillain-Barré syndrome (GBS), who later developed clinical and ...
Itay, Lotan   +3 more
openaire   +2 more sources

MORVAN'S SYNDROME : A RARE CASE REPORT

INTERNATIONAL JOURNAL OF SCIENTIFIC RESEARCH, 2023
Morvan's syndrome is an autoimmune disorder characterized by central, autonomic, and peripheral hyperactivity with associated thymoma in majority. The clinical features include insomnia, hyperhidrosis, myokymia, dysautonomia and hallucinations. Voltage gated potassium channel (VGKC) namely, leucine-rich glioma inactivated 1 (LGI-1) antibody and ...
Chandan Zha   +3 more
openaire   +1 more source

Autoimmune encephalitis and Morvan’s syndrome

2020
Abstract Since its first recognition in 2001, hundreds of patients have been identified with autoimmune limbic encephalitis (LE) associated with antibodies that immunoprecipitate voltage-gated potassium channel (VGKC)-complex proteins.
Camilla Buckley, Angela Vincent
openaire   +1 more source

A Case Report: Morvan's Syndrome

Research Journal of Pharmacy and Technology, 2017
Morvan’s syndrome is a rare autoimmune disorder showing peripheral nervous system hyperexcitability accompanied by autonomic and central nervous system (CNS) hyperactivity. Peripheral hyperactivity includes clinical and electrophysiological evidence of painful cramps, myokymia and neuromyotonia.
S Sreeni   +2 more
openaire   +1 more source

Fatal Morvan Syndrome Associated With Myasthenia Gravis

The Neurologist, 2017
Introduction: Morvan syndrome is a rare and complex autoimmune disorder affecting multiple sites of neuraxis. Case Report: We present fulminant Morvan syndrome, developing on a background of chronic myasthenia gravis.
Madhu, Nagappa   +7 more
openaire   +2 more sources

A Case Report Of Morvan Syndrome

2020
Electromyography and neurotransmission examination results were concordant with peripheral nerve hyperreactivity. Contactin-associated protein-like 2 antibodies and leucine-rich glioma inactivated protein 1 antibodies were detected as positive. The patient was diagnosed with Morvan syndrome; intravenous immunoglobulin and corticosteroid treatment was ...
Sakarya Üniversitesi/Tıp Fakültesi/Dahili Tıp Bilimleri Bölümü   +3 more
openaire   +1 more source

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