نتایج جستجو برای: childhood guillain

تعداد نتایج: 166044  

Journal: :Lancet 2016
Hugh J Willison Bart C Jacobs Pieter A van Doorn

Guillain-Barré syndrome is the most common and most severe acute paralytic neuropathy, with about 100,000 people developing the disorder every year worldwide. Under the umbrella term of Guillain-Barré syndrome are several recognisable variants with distinct clinical and pathological features. The severe, generalised manifestation of Guillain-Barré syndrome with respiratory failure affects 20-30...

2010
Maria Colantuoni Elide Matano Salvatore Alfieri Sabino De Placido Chiara Carlomagno

Guillain-Barre syndrome is a rare clinical entity classified as an ascending muscle paralysis led by autonomic nervous dysfunction due to autoimmune damage of peripheral nerves. Paraneoplastic Guillain-Barre syndrome has been described in association with some kinds of tumors (B-cell Lymphoma and small cell lung cancer). We describe the case of a 74-year-old woman affected by gastric adenocarci...

2013
Benjamin Kloesel LaTonya J. Hickson

Guillain-Barré syndrome is an immune-mediated polyneuropathy that frequently presents with progressive muscle weakness. Hyponatremia has recently been described as a feature of this condition, generally appearing over the course of the illness and following the diagnosis of this demyelinating process. We report a case of Guillain-Barré syndrome presenting with severe hyponatremia that is furthe...

2003
B C Jacobs P A van Doom J H M Groeneveld

To investigate whether antecedent cytomegalovirus (CMV) infections in patients with Guillain-Barre syndrome are associated with the presence of specific antiganglioside antibodies, acute phase serum samples from 130 patients with Guillain-Barre syndrome and 200 controls were tested. Anti-GM2 IgM antibodies were found more often in patients with Guillain-Barre syndrome with CMV infection (22%) t...

2010
Mary L Stevenson Louis H Weimer Ilya V Bogorad

INTRODUCTION Guillain-Barré syndrome is an immune-mediated polyneuropathy that is routinely initially treated with either intravenous immunoglobulin or plasmapheresis. To the best of our knowledge, no association between plasmapheresis treatment and acute onset of facial neuropathy has been reported. CASE PRESENTATION A 35-year-old Caucasian man with no significant prior medical history devel...

1999
J Duarte A Cruz Martinez F Rodriguez A Mendoza A P Sempere L E Claveria

Hereditary motor and sensory neuropathy (HMSN) types I and III and chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) in developed countries are the most frequent causes of enlargement of peripheral nerves, “hypertrophic neuropathy”, with clinically palpable thickened nerves, visible on MRI. They may even be the cause of spinal cord compression. 8 We report on a patient who develo...

Journal: :Journal of neurology, neurosurgery, and psychiatry 1999
J Duarte A C Martinez F Rodriguez A Mendoza A P Sempere L E Claveria

Hereditary motor and sensory neuropathy (HMSN) types I and III and chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) in developed countries are the most frequent causes of enlargement of peripheral nerves, “hypertrophic neuropathy”, with clinically palpable thickened nerves, visible on MRI. They may even be the cause of spinal cord compression. 8 We report on a patient who develo...

2016
Rajkumar M. Meshram S. Abhisheik Hina Agrawal Samadhan Dhakne

Guillain Barre Syndrome (GBS) off late has been the most frequent cause of acute flaccid paralysis worldwide, replacing poliomyelitis which dominated in the past few decades. A 4 months old female infant was presented with sudden onset; nonprogressive weakness of both lower limbs with areflexia and urinary retention such clinical features consistent with Guillain Barre Syndrome. She was treated...

Journal: :European review for medical and pharmacological sciences 2014
P Pavone A Le Pira F Greco G Vitaliti P L Smilari E Parano R Falsaperla

Three young patients with Bickerstaff's brainstem encephalitis (BBE) are reported. Some weeks following an upper tract infection, the children after a short period of recovery, showed acute onset of symmetric weakness of the lower limbs with difficulty in standing by and walking. The distal muscle weakness had a rapid progression with involvement of the cranial nerve, and then with severe impai...

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