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Dergiler / Erciyes Medical Journal / 2015 / Cilt: 37 - Sayı: 2

Severe Pure Acute Motor Axonal Neuropathy

Nebahat TAŞDEMİR
Mehmet KARAKOÇ
PELİN OKTAYOĞLU
Kemal NAS
Sayfa
81–84
DOI
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Yapay Zeka Hızlı Bakış & Çıkarımlar

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⚡ TL;DR(1 Cümlede Hızlı Çıkarım)

Neurologists and physiatrist should conduct long term monitoring and rehabilitation for patients with AMAN because neurological deficits may persist for a long time.

📌 3 Maddede Bu Makale

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Amaç & Hipotez:Acute motor axonal neuropathy (AMAN) is a subtype of Guillain–Barré syndrome.
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Temel Bulgular & Veri:Our patient described progressive weakness in his leg and was not able to independently walk; he had a feeling weakness in his arms within 24 h after the onset of symptoms.
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Sonuç & Katkı:Neurologists and physiatrist should conduct long term monitoring and rehabilitation for patients with AMAN because neurological deficits may persist for a long time.
🔬Tür:Araştırma Makalesi
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler:Alan Parametreleri

Abstract

Acute motor axonal neuropathy (AMAN) is a subtype of Guillain–Barré syndrome. Characteristic electrophysiological features of AMAN are reduced amplitude or absence of muscle action potentials. Our patient described progressive weakness in his leg and was not able to independently walk; he had a feeling weakness in his arms within 24 h after the onset of symptoms. He was diagnosed with AMAN according to the clinical and electrophysiological features. He could independently walk after two years following intensive physical therapy and monitoring. Neurologists and physiatrist should conduct long term monitoring and rehabilitation for patients with AMAN because neurological deficits may persist for a long time.

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Bu Makaleye Atıf Yap

TAŞDEMİR, N., KARAKOÇ, M., OKTAYOĞLU, P., NAS, K. (2015). Severe Pure Acute Motor Axonal Neuropathy. Erciyes Medical Journal, Cilt: 37 - Sayı: 2, 81–84. https://ajindex.com/articles/223502

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Kaynakça (3)

  1. JB Winer. Guillain-Barré Syndrome. Journal of Clinical Pathology: Mol Pathol 2001; 54(6): 381-5
  2. McKhann GM, Cornblath DR, Griffin JW, Ho TW, Li CY, Jiang Z, et al. Acute motor axonal neuropathy: a frequent cause of acute flaccid paralysis in China. Ann Neurol 1993; 33(4): 333-42. [CrossRef] 3. Hiraga A,Mori M, Ogawara K, S Kojima, T Kanesaka, S Misawa et al. Re- covery patterns and long term Prognosis for axonal Gillain Barre syndrome. J Neurol Neurosurgary Psychiatry 2005; 76(5): 719-22. [CrossRef] 4. Kokubun N, Nishibayashi M, Uncini A, Odaka M, Hirata K, Yuki N. Conduction block in acute motor axonal neuropathy. Brain 2010; 133(10): 2897-908. [CrossRef] 5. Korinthenberg R, Schessl J, Kirschner J. Clinical presentation and course of childhood Guillain-Barré syndrome: a prospective multicen- tre study. Neuropediatrics 2007; 38(1): 10-7. [CrossRef] 6. Ryan MM. Guillain-Barré syndrome in childhood. J Pediatr Child Health 2005; 41(5-6): 237-41. [CrossRef] 7. Hughes RAC, Raphael JC, Swan AV, van Doorn PA. Intravenous ımmunoglobulin for Guillain-Barré syndrome (Cohcrane Review ). Co- chrane Database of Systemic Reviews 2001;2 CD002063
  3. Van der Meché FG, Visser LH, Jacobs BC, Endtz HP, Meulstee J, van Doorn PA. Guillain-Barré syndrome: multifactorial mechanisms versus de- fined subgroups. J Infect Dis 1997; 176(Suppl 2): 99-102. [CrossRef] 9. Nagasawa K, Kuwabara S, Misawa S, Fujii K, Tanabe Y, Yuki N, et al. Electrophysiological subtypes and prognosis of childhood Guillain-Barré syndrome in Japan. Muscle Nerve 2006; 33(6): 766-70. [CrossRef] 10. Devos D, Magot A, Perrier-Boeswillwald J, Fayet G, Leclair-Vison- neau L, Ollivier Y et al. Guillain-Barré syndrome during childhood: particular clinical and electrophysiological features. Muscle Nerve 2013; 48(2): 247-51. [CrossRef]