Results 201 to 210 of about 31,200 (259)

Pain in acute motor axonal neuropathy

Muscle & Nerve, 2021
AbstractIntroduction/AimsPatients with acute motor axonal neuropathy (AMAN) generally have pure motor neuropathy and clinicians usually do not link pain with AMAN. The aim of this retrospective study was to describe the character, location, and intensity of pain in AMAN and acute inflammatory demyelinating polyneuropathy (AIDP) in the acute phase ...
Fei Zhao, Juan Wang, Jing Zhang, Xiaomin Pang, Shan Huang, Xueli Chang, Junhong Guo, Wei Zhang   +7 more
openaire   +3 more sources

Claw Hand in Acute Motor Axonal Neuropathy Variant

Journal of The Association of Physicians of India
Guillain-Barré syndrome (GBS) is an acute autoimmune polyradiculoneuropathy with various subtypes, including the acute motor axonal neuropathy (AMAN) variant. Distal muscle weakness is typically rare in AMAN. Myositis, an inflammatory muscle condition, is infrequently documented in GBS.
M, Chozhan, P, Vishaal, Gurunathan, Srinivasan, Lakshmanan, Sankaranarayanan, Mugundhan, Krishnan   +4 more
openaire   +3 more sources

Systemic Lupus Erythematosus Initially Presenting as Acute Motor and Sensory Axonal Neuropathy Variant of Guillain-Barre Syndrome in a Healthy Active Duty Female.

Military Medicine, 2023
Guillain-Barre syndrome (GBS) is an acute monophasic immune-mediated polyradiculoneuropathy characterized by rapidly evolving ascending weakness, mild sensory loss, and hypo- or areflexia, typically progressing to peak symptoms over the course of 4 weeks.
Samantha Braun, Luisa Bastian, Corey Hayes, S. Owen, Cassandra Craig, Alexis Nelson   +5 more
semanticscholar   +1 more source

Acute motor axonal neuropathy and acute motor-sensory axonal neuropathy share a common immunological profile

Journal of the Neurological Sciences, 1999
Griffin and colleagues (Griffin JW, Li CY, Ho TW, Tian M, Gao CY, Xue P, Mishu B, Cornblath DR, Macko C, McKhann GM, Asbury AK. Pathology of motor-sensory axonal Guillain-Barré syndrome. Ann Neurol 1996;39:17-28 [4]) proposed that acute motor axonal neuropathy (AMAN) and acute motor-sensory axonal neuropathy (AMSAN) are part of the spectrum of a single
N, Yuki, S, Kuwabara, M, Koga, K, Hirata
openaire   +2 more sources

Acute Motor Axonal Neuropathy–An Atypical Presentation

Pediatric Neurology, 2007
Guillain-Barré syndrome, an autoimmune disorder of the peripheral nervous system, is divided into several subtypes according to clinico-pathologic findings and epidemiologic characteristics. A pure motor variant without involvement of the sensory nerves has been reported in rare cases.
Yuval E, Landau, Ron, Dabby, Jacob, Amir, Rachel, Straussberg   +3 more
openaire   +2 more sources

Dry Beriberi and Acute Motor-Sensory Axonal Neuropathy-Induced Paralysis: A Case Report

Cureus
Acute motor-sensory axonal neuropathy (AMSAN) is a variant of Guillain-Barré syndrome (GBS) and a rare cause of paralysis. AMSAN can present similarly to axonal neuropathy caused by thiamine (vitamin B1) deficiency, which is known as dry beriberi. Subtle
Marcelo Salazar, Awab Elnaeem, Xiang Fang   +2 more
semanticscholar   +1 more source

Acute Motor Axonal Neuropathy

2017
Acute motor axonal neuropathy (AMAN) is a pure motor axonal subtype of Guillain–Barre syndrome (GBS). In Asia and Central and South America, it is a major subtype of GBS. AMAN progresses more rapidly and has an earlier peak than demyelinating GBS; tendon reflexes are relatively preserved or even exaggerated, and autonomic dysfunction is rare. Molecular
Satish V. Khadilkar, Rakhil S. Yadav, Bhagyadhan A. Patel   +2 more
openaire   +1 more source

Time course of axonal regeneration in acute motor axonal neuropathy

Muscle & Nerve, 2007
AbstractPatients with acute motor axonal neuropathy (AMAN) generally recover well. We reviewed clinical and electrophysiologic recovery in 13 patients for up to 5 years. Twelve patients showed rapid recovery over 12 months, whereas in the remaining one the recovery was slow and incomplete at 5 years.
Noriko, Tamura, Satoshi, Kuwabara, Sonoko, Misawa, Kazuaki, Kanai, Miho, Nakata, Setsu, Sawai, Masahiro, Mori, Takamichi, Hattori   +7 more
openaire   +2 more sources

Understanding hyper-reflexia in acute motor axonal neuropathy (AMAN)

Neurophysiologie Clinique, 2020
Hyper-reflexia is occasionally seen in acute motor axonal neuropathy (AMAN), but its pathophysiology is unclear. We report a patient with AMAN following Campylobacter jejuni enteritis, who showed generalized hyper-reflexia, bilateral Hoffmann sign and right Babinski sign.
Versace V., Campostrini S., Rastelli E., Sebastianelli L., Nardone R., Pucks-Faes E., Saltuari L., Kofler M., Uncini A.   +8 more
openaire   +2 more sources

Cerebral white matter lesions in acute motor axonal neuropathy

Neurology, 2003
In acute motor axonal neuropathy (AMAN), deep tendon reflexes are occasionally preserved or exaggerated,1-5⇓⇓⇓⇓ although the mechanism is unknown. We report the first known patient with AMAN presenting hyperreflexia in whom a CNS lesion was detected by MRI.
K, Sekiguchi, K, Susuki, I, Funakawa, K, Jinnai, N, Yuki   +4 more
openaire   +2 more sources