An Acute Motor Axonal Neuropathy (AMAN) case with motor conduction blocks in childhood

ArticleAçık Erişim

Özet

Objective Acute motor axonal neuropathy (AMAN), 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 Kirdar 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. © 2016, Iranian Child Neurology Society. All rights reserved.

Anahtar Kelimeler

RDL Kalıcı Bağlantı (PID)
https://rdlopen.rawdatalibrary.net/r/ebyu/15042Resmi atıflarda kullanılan kalıcı adres
Tam Kayıt
AlanDeğerDil
dc.contributor.authorYildirim, Serhan
dc.contributor.authorIna, Rahşan Adviye
dc.contributor.authorGül, Hakan Levent
dc.contributor.authorBörü, Ülkü Türk
dc.date.accessioned2026-10-18T20:29:50.052770646Z
dc.date.available2026-10-18T20:29:50.052770646Z
dc.date.issued2016
dc.description.abstractObjective Acute motor axonal neuropathy (AMAN), 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 Kirdar 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. © 2016, Iranian Child Neurology Society. All rights reserved.
dc.identifier.endpage69
dc.identifier.issn1735-4668
dc.identifier.issue1
dc.identifier.scopus2-s2.0-84952838007
dc.identifier.startpage65
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/ebyu/15042
dc.identifier.volume10
dc.language.isoen
dc.publisherIranian Child Neurology Society
dc.relation.ispartofIranian Journal of Child Neurology
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectAcute motor axonal neuropathy
dc.subjectGuillain-barre syndrome
dc.subjectMotor conduction blocks
dc.subjectareflexia
dc.subjectArticle
dc.subjectcase report
dc.subjectchild
dc.subjectdysarthria
dc.subjectdysphagia
dc.subjectdysphonia
dc.subjectelectromyography
dc.subjectelectrophysiology
dc.subjecteye movement disorder
dc.subjecthuman
dc.subjectmale
dc.subjectmotor nerve conduction
dc.subjectnerve conduction disorder
dc.subjectneurologic examination
dc.subjectperipheral nerve
dc.subjectpolyradiculoneuropathy
dc.subjectposterior tibial nerve
dc.subjectpreschool child
dc.subjectquadriplegia
dc.subjectserology
dc.subjectweakness
dc.titleAn Acute Motor Axonal Neuropathy (AMAN) case with motor conduction blocks in childhood
dc.typeArticle
dspace.entity.typePublication
rdl.citation.scopus4
rdl.source.indexSCOPUS