نتایج جستجو برای: acute motor axonal neuropathy

تعداد نتایج: 700825  

Journal: :Indian journal of pediatrics 2010
Sunil Gomber Pooja Dewan Devender Chhonker

Ten out of 20 children, treated with usual doses of vincristine for various types of childhood cancers, developed neurotoxicity during treatment. Peripheral neurotoxicity (mixed motor-sensory 4/10, pure motor 3/10, pure sensory 3/10) was seen in the form of weakness of lower limbs, areflexia, neuropathic pain, or sensory loss. Autonomic neuropathy presented as constipation and urinary retention...

2010
Heung-Yong Jin Kyung-Ae Lee So-Young Kim Ji-Hyun Park Hong-Sun Baek Tae-Sun Park

A 59-year-old man was admitted with numbness, pain, and a tingling sensation in both lower legs. He was initially diagnosed with diabetic peripheral neuropathy based on a symptom questionnaire and a quantitative sensory test. Despite symptomatic treatment of diabetic neuropathy, he complained of worsening sensory symptoms and additional motor weakness in both lower extremities. As the motor wea...

2013
Kiyokazu OZAKI Shotaro YAMANO Tetsuro MATSUURA Isao NARAMA

Rodent models of diabetes develop a slowing of nerve conduction velocity and mild axonal atrophy, but generally lack overt degenerative neuropathy. Spontaneously diabetic Wistar Bonn Kobori (WBN/Kob) rats develop severe diabetic peripheral motor neuropathy with a slowing of nerve conduction velocity. We examined the effect of glycemic control, using insulin implant, on neuropathic changes in th...

Journal: :Brain & development 2008
José L Fernández-Torre José L Teja Alvaro Castellanos Javier Figols Tomás Obeso Rosa Arteaga

We report the case of a neonate with spinal muscular atrophy type I (SMA type I or Werdnig-Hoffman disease) who was initially misdiagnosis as having critical illness neuropathy. Electromyography (EMG) showed a moderate loss of voluntary and motor unit potentials of both neurogenic and myopathic appearance. Nerve conduction studies revealed the presence of a severe sensory-motor axonal neuropath...

Journal: :Journal of medical genetics 1988
J L Tolmie D E Wilcox R McWilliam A Assindi J B Stephenson

Autosomal dominant inheritance of a syndrome comprising palmoplantar keratoderma, nail dystrophy, and hereditary motor and sensory neuropathy (HMSN) was observed in three generations of one family. Nail dystrophy affected the toe and fingernails; it was present at birth or developed during early childhood. Palmoplantar keratoderma became apparent in later childhood. Each subject with nail dystr...

Journal: :Practical neurology 2015
Alexander M Rossor Matthew R B Evans Mary M Reilly

Charcot-Marie-Tooth disease is the commonest inherited neuromuscular disease. It is characterised by degeneration of peripheral sensory and motor nerves and can be classified into axonal and demyelinating forms. This review provides a diagnostic approach to patients with suspected inherited neuropathy and an algorithm for genetic testing that includes recent advances in genetics such as next-ge...

Journal: :AJNR. American journal of neuroradiology 2011
H-F Li X-J Ji

Enhanced MR Imaging in Guillain-Barré Syndrome Although we appreciate the excellent images of enhanced cranial nerves in pediatric patients with Guillain-Barré syndrome (GBS) and their contribution to the understanding of GBS as a continuum rather than distinct entities, we do not agree with Zuccoli et al that brain MR imaging should be considered in the routine evaluation in pediatric patients...

Journal: :The Southeast Asian journal of tropical medicine and public health 1998
M Isaäcson

Campylobacter infection of the gastrointestinal tract has been observed as an antecedent illness in some patients with Guillain-Barre syndrome (GBS); these patients have been reported to have poor prognosis. We investigated 29 patients with GBS, admitted to our hospital from January 1996 to December 1999 for recent Campylobacter enteritis by culture of their stool specimens. Campylobacter upsal...

Journal: :Neurology 2012
Robert D S Pitceathly Sinéad M Murphy Ellen Cottenie Annapurna Chalasani Mary G Sweeney Cathy Woodward Ese E Mudanohwo Iain Hargreaves Simon Heales John Land Janice L Holton Henry Houlden Julian Blake Michael Champion Frances Flinter Stephanie A Robb Rupert Page Michael Rose Jacqueline Palace Carol Crowe Cheryl Longman Michael P Lunn Shamima Rahman Mary M Reilly Michael G Hanna

OBJECTIVE Charcot-Marie-Tooth (CMT) disease is the most common inherited neuromuscular disorder, affecting 1 in 2,500 individuals. Mitochondrial DNA (mtDNA) mutations are not generally considered within the differential diagnosis of patients with uncomplicated inherited neuropathy, despite the essential requirement of ATP for axonal function. We identified the mtDNA mutation m.9185T>C in MT-ATP...

Journal: :Practical neurology 2015
Antonino Uncini

To cite: Uncini A. Pract Neurol 2015;15:88–89. Wakerley and Yuki report the wide heterogeneity of the clinical spectrum of Guillain–Barré syndrome (GBS), highlighting atypical presentations and reviewing the differential diagnoses. The approach is practical and their intent is to facilitate early diagnosis and treatment without relying on laboratory and electrophysiological findings. It is near...

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