نتایج جستجو برای: childhood guillain

تعداد نتایج: 166044  

Ahmadfard, Parivash, Aramesh fard, Shideh, Ebrahimi, Mohammad mehdi, Khazforoosh, Sahar, Manafi, Alireza, Mossallaiepoor, Ali, Mousaei, N, Rahimi jaberi, Abbas, Salami, Javad, Shirazi zade mehraban, Shadan,

Background &Objective: Guillain Barre´ syndrome is an autoimmune neuropathy which is considered to be the most acute areflexic paralysis with albuminocytologic dissociation.1 Areflexia or hyporeflexia, pain in limbs, autonomic dysfunction, progressive bilateral and symmetric weakness of limbs, numbness and paresthesia are described as the clinical features of GBS.Nevertheless, with having less ...

2016
Motohiro Matsui Mariko Shimizu Aya Ioi Azusa Mayumi Kohei Higuchi Akihisa Sawada Maho Sato Masahiro Yasui Keiko Yanagihara Masami Inoue

A 16-month-old girl was diagnosed with Epstein-Barr virus hemophagocytic lymphohistiocytosis and transferred to our hospital on the 58th day of the hemophagocytic lymphohistiocytosis after treatment failure according to the Hemophagocytic Lymphohistiocytosis-2004 protocol. On admission to our hospital, she had a flaccid paralysis of her lower limbs. Nerve conduction studies showed a acute motor...

2013
P Hantson X Wittebole P Van Den Bergh

Abstract Introduction This article reports a case of the difficulty to differentiate between critical illness polyneuropathy and axonal Guillain–Barré syndrome when triggered by subarachnoid haemorrhage. Case report An 81-year-old man was admitted comatose (Glasgow coma scale score 4/15) after a subarachnoid haemorrhage. His neurological condition gradually improved with as best motor response ...

Journal: :Clinical neuropharmacology 2005
Julián Benito-León Alex J Mitchell

Olanzapine is the most commonly prescribed atypical antipsychotic drug. Recently there has been increased concern over possible adverse metabolic effects of this drug. The authors describe the first case of Guillain-Barré-like syndrome associated with an olanzapine hypersensitivity reaction. The presence of progressive numbness, motor weakness, or pain in the limbs of patients receiving olanzap...

Journal: :The Journal of the Association of Physicians of India 2007
Vandana Talwar Neelkamal Mehndiratta P K Verma

Barium poisoning is an important cause of areflexic quadriplegia associated with hypokalemia. Presenting features may mimic Guillain-Barre syndrome. A high index of suspicion of barium poisoning in two patients who presented with features resembling Guillain-Barre syndrome, led to timely management and early recovery in both the cases.

2008

)ften difficult. Often, clinical tésting of the sensory :uflctions is neither reliable nor helpful in the determination. Theoretically, predominant proximal . veakness, neck flexor weakness, and facial weakness occur more often in patients with myopathy. Dn needle electromyography, low amplitudes and short duration of the motor unit potentials suggest myopathy. Normal sensory nerve action poten...

Journal: :acta medica iranica 0
k. sadeghniat g. pooryaghoob e. rafeemanesh

n-hexane neuropathy has been described after glue sniffing and industrial exposure. onset may be subacute and reminiscent of guillain-barre' syndrome. five patients (15-18 years old) presented with paresthesia, severe weakness of the extremities particularly lower extremities, as well as muscular atrophy, total areflexia and gait disturbances were admitted in hospital in march 2003. all of thes...

Journal: :AANA journal 1994
M E Plaugher

A case study is presented of a 20-year-old male with a recent exacerbation of Guillain-Barré syndrome who had an emergent exploratory laparotomy under general endotracheal anesthesia. His preoperative history and physical examination indicated complicating factors, including blunt abdominal trauma, ethanol ingestion, and a full stomach. The management of patients with Guillain-Barré syndrome an...

Journal: :Neurosciences 2002
Roshan L Koul Parameswaran M Nair Alexander Chacko Poothirikovil Venugopalan

A 10-year-old girl with Fischer`s variant of acute Guillain-Barre syndrome is described. She had predominantly sensory involvement with autonomic dysfunction, ophthalmoplegia and myoclonic jerks. Myoclonus persisted for 2 weeks and the pupillary involvement was evident even after 2 months. The association of myoclonus with Guillain-Barre syndrome has not been previously reported.

Journal: :Cases Journal 2008
Ram Prakash Narayanan Nirmal James Kannan Ramachandran Mario J Jaramillo

Bilateral paralysis of the facial nerve is a relatively rare presentation and often indicates a serious underlying medical condition. Guillain-Barré syndrome needs to be considered, among others in the differential diagnoses of such presentation. We present here the case of a 35 year old female who presented with bilateral facial nerve paralysis due to the Guillain-Barré syndrome.

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