Results 121 to 130 of about 1,153,947 (162)
Morvan Syndrome Following B-cell Lymphoma
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
Some of the next articles are maybe not open access.
Related searches:
Related searches:
Morvan's syndrome: Clinical, laboratory, and in vitro electrophysiological studies
Muscle and Nerve, 2004AbstractMorvan'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, 2004This 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, 2008Morvan'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, 2016Morvan'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, 2023Morvan'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
2020Abstract 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, 2017Morvan’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, 2017Introduction: 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
2020Electromyography 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

