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Vol. 10 No. 1 (2016)

January 2016

Acute Motor Axonal Neuropathy (Aman) With Motor Conduction Blocks In Childhood; Case Report

  • Serhan YILDIRIM
  • RahÅŸan Adviye İNAN
  • Hakan Levent GÜL
  • Ülkü TÜRK BÖRÜ

Iranian Journal of Child Neurology, Vol. 10 No. 1 (2016), 1 January 2016 , Page 70-72
https://doi.org/10.22037/ijcn.v10i1.6973 Published: 2016-01-01

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Abstract

How to Cite This Article: Yıldırım S. Inan AR, Gül LH, Türk Börü Ü. An Acute Motor Axonal Neuropathy (AMAN) Case With Motor Conductıon Blocks In Childhood. Iran J Child Neurol. Winter 2016; 10(1):65-69.

Abstract

Objective

characterized with decreased compound muscle action potentials (CMAP) and absence of demyelinating findings in electrophysiological studies, is a subtype of Guillain-Barre Syndrome (GBS). A 4 yr-old male patient presented with ascending weakness, dysarthria and dysphagia to İstanbul Dr. Lütfi Kırdar Kartal Training and Research Hospital Neurology outpatient for three days to in 2012. Dysphonia, restricted eye movements, flaccid tetraplegia and areflexia were found in neurological examination. There were motor conduction blocks in all peripheral nerves in electrophysiological studies.According to these findings the patient was diagnosed as Acute Inflammatory Demyelinating Polyradiculoneuropathy (AIDP). Reduction of CMAP amplitudes in posterior tibial nerve, absence of CMAPs in median, ulnar and peroneal nerves and loss of motor conduction blocks were found in following electrophysiological studies. According to these findings, patient was diagnosed as AMAN. Motor conduction blocks may appear in early stage of AMAN and they disappear in later examinations.

That’s why electrophysiological studies must be repeated in patients with GBS.

Keywords:
  • Acute motor axonal neuropathy
  • Motor conduction blocks
  • Guillain-Barre Syndrome
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How to Cite

YILDIRIM, S., İNAN, R. A., GÜL, H. L., & TÜRK BÖRÜ, Ülkü. (2016). Acute Motor Axonal Neuropathy (Aman) With Motor Conduction Blocks In Childhood; Case Report. Iranian Journal of Child Neurology, 10(1), 70–72. https://doi.org/10.22037/ijcn.v10i1.6973
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