Lesion Localization and Prognosis Using Electrodiagnostic Studies in Facial Diplegia: A Rare Variant of Guillain-Barre Syndrome
BackgroundThe etiology of facial nerve palsy is diverse and includes herpes zoster virus, Guillain-Barre syndrome (GBS), otitis media, Lyme disease, sarcoidosis, human immunodeficiency virus, etc. The lower motor neuron type facial nerve palsy is usually caused by an ipsilateral facial nerve lesion;...
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description | BackgroundThe etiology of facial nerve palsy is diverse and includes herpes zoster virus, Guillain-Barre syndrome (GBS), otitis media, Lyme disease, sarcoidosis, human immunodeficiency virus, etc. The lower motor neuron type facial nerve palsy is usually caused by an ipsilateral facial nerve lesion; however, it may be caused by a central lesion of the facial nerve nucleus and tract in the pons. Facial diplegia is an extremely rare condition that occurs in approximately 0.3% to 2.0% of all facial palsies. Electrodiagnostic studies including direct facial nerve conduction, facial electromyography (EMG), and blink reflex studies are useful for the prognosis and lesion localization in facial nerve palsy.MethodologyThis retrospective, observational study was conducted at the Neurophysiology Unit, Hamad General Hospital, Doha, Qatar. This study included 11 patients with bilateral facial weakness who visited for electrodiagnostic studies in the neurophysiology laboratory.ResultsIn total, eight (72.7%) patients had facial diplegia, eight (72.7%) had hypo/areflexia, seven (63.6%) had facial numbness, and five (45.5%) had cerebrospinal fluid albuminocytological dissociation. The most frequent cause of facial diplegia in this study was GBS (81.9%). Direct facial nerve conduction stimulation showed that nine (81.8%) patients had bilateral facial nerve low compound muscle action potential amplitudes. The bilateral blink reflex study showed that eight (88.8%) patients had absent bilateral evoked responses. Finally, the EMG study showed that five (55.5%) patients had active denervation in bilateral sample facial muscles.ConclusionsBilateral facial nerve palsy is an extremely rare condition with a varied etiology. Electrodiagnostic studies are useful in detecting the underlying pathophysiologic processes, prognosis, and central or peripheral lesion localization in patients with facial diplegia. |
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fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_9200109</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2678745324</sourcerecordid><originalsourceid>FETCH-LOGICAL-c276t-62f565daa4be67654b458144a741a38b5b9eee8d88aaefec2af06ea2bb96ef6f3</originalsourceid><addsrcrecordid>eNpdkU1v1DAQhiMEolXpjR9giQsHUmzHX-GAVEpbkFYCUcrVmjiTZaqsvdgJUnvhrzfLVgg4zdejVzPzVtVzwU-s1e3rMGecy4nUXNlH1aEUxtVOOPX4r_ygOi7lhnMuuJXc8qfVQaOtaG2rD6tfKyyUIlulACPdwbQrIPbsc07rmAoVdl0ortn5iGHKqSfYtScK7Gqae8LCKLILCAQje0_bEdcEb9gp-wIZ2TfIBHFiaWCXM40jUKzfQV4mV7exz2mDz6onA4wFjx_iUXV9cf717EO9-nT58ex0VQdpzVQbOWijewDVobFGq05pJ5QCqwQ0rtNdi4iudw4ABwwSBm4QZNe1BgczNEfV273udu422AeMU4bRbzNtIN_6BOT_nUT67tfpp2_l7nHtIvDyQSCnHzOWyW-oBFxuipjm4qWxzirdSLWgL_5Db9Kc43LeQjlptDZCLtSrPRVyKiXj8GcZwf3OXL831_82t7kH28GaDw</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2682655612</pqid></control><display><type>article</type><title>Lesion Localization and Prognosis Using Electrodiagnostic Studies in Facial Diplegia: A Rare Variant of Guillain-Barre Syndrome</title><source>PubMed Central Open Access</source><source>PubMed Central</source><creator>Ali, Liaquat ; Alhatou, Mohammed ; Adeli, Gholam ; Elalamy, Osama ; Zada, Yasin ; Mohammed, Imran ; Sharif, Muhammad ; Noor Illahi, Memon ; Naeem, Muhammad ; Iqrar, Ambreen</creator><creatorcontrib>Ali, Liaquat ; Alhatou, Mohammed ; Adeli, Gholam ; Elalamy, Osama ; Zada, Yasin ; Mohammed, Imran ; Sharif, Muhammad ; Noor Illahi, Memon ; Naeem, Muhammad ; Iqrar, Ambreen</creatorcontrib><description>BackgroundThe etiology of facial nerve palsy is diverse and includes herpes zoster virus, Guillain-Barre syndrome (GBS), otitis media, Lyme disease, sarcoidosis, human immunodeficiency virus, etc. The lower motor neuron type facial nerve palsy is usually caused by an ipsilateral facial nerve lesion; however, it may be caused by a central lesion of the facial nerve nucleus and tract in the pons. Facial diplegia is an extremely rare condition that occurs in approximately 0.3% to 2.0% of all facial palsies. Electrodiagnostic studies including direct facial nerve conduction, facial electromyography (EMG), and blink reflex studies are useful for the prognosis and lesion localization in facial nerve palsy.MethodologyThis retrospective, observational study was conducted at the Neurophysiology Unit, Hamad General Hospital, Doha, Qatar. This study included 11 patients with bilateral facial weakness who visited for electrodiagnostic studies in the neurophysiology laboratory.ResultsIn total, eight (72.7%) patients had facial diplegia, eight (72.7%) had hypo/areflexia, seven (63.6%) had facial numbness, and five (45.5%) had cerebrospinal fluid albuminocytological dissociation. The most frequent cause of facial diplegia in this study was GBS (81.9%). Direct facial nerve conduction stimulation showed that nine (81.8%) patients had bilateral facial nerve low compound muscle action potential amplitudes. The bilateral blink reflex study showed that eight (88.8%) patients had absent bilateral evoked responses. Finally, the EMG study showed that five (55.5%) patients had active denervation in bilateral sample facial muscles.ConclusionsBilateral facial nerve palsy is an extremely rare condition with a varied etiology. Electrodiagnostic studies are useful in detecting the underlying pathophysiologic processes, prognosis, and central or peripheral lesion localization in patients with facial diplegia.</description><identifier>ISSN: 2168-8184</identifier><identifier>EISSN: 2168-8184</identifier><identifier>DOI: 10.7759/cureus.25047</identifier><identifier>PMID: 35719795</identifier><language>eng</language><publisher>Palo Alto: Cureus Inc</publisher><subject>Ataxia ; Diagnostic tests ; Dysarthria ; Dysphagia ; Electromyography ; Guillain-Barre syndrome ; Internal Medicine ; Lyme disease ; Medical prognosis ; Neurological disorders ; Neurology ; Neurophysiology ; Proteins ; Viral infections</subject><ispartof>Curēus (Palo Alto, CA), 2022-05, Vol.14 (5), p.e25047-e25047</ispartof><rights>Copyright © 2022, Ali et al. This work is published under https://creativecommons.org/licenses/by/3.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>Copyright © 2022, Ali et al. 2022 Ali et al.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c276t-62f565daa4be67654b458144a741a38b5b9eee8d88aaefec2af06ea2bb96ef6f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9200109/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9200109/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,315,728,781,785,886,27929,27930,53796,53798</link.rule.ids></links><search><creatorcontrib>Ali, Liaquat</creatorcontrib><creatorcontrib>Alhatou, Mohammed</creatorcontrib><creatorcontrib>Adeli, Gholam</creatorcontrib><creatorcontrib>Elalamy, Osama</creatorcontrib><creatorcontrib>Zada, Yasin</creatorcontrib><creatorcontrib>Mohammed, Imran</creatorcontrib><creatorcontrib>Sharif, Muhammad</creatorcontrib><creatorcontrib>Noor Illahi, Memon</creatorcontrib><creatorcontrib>Naeem, Muhammad</creatorcontrib><creatorcontrib>Iqrar, Ambreen</creatorcontrib><title>Lesion Localization and Prognosis Using Electrodiagnostic Studies in Facial Diplegia: A Rare Variant of Guillain-Barre Syndrome</title><title>Curēus (Palo Alto, CA)</title><description>BackgroundThe etiology of facial nerve palsy is diverse and includes herpes zoster virus, Guillain-Barre syndrome (GBS), otitis media, Lyme disease, sarcoidosis, human immunodeficiency virus, etc. The lower motor neuron type facial nerve palsy is usually caused by an ipsilateral facial nerve lesion; however, it may be caused by a central lesion of the facial nerve nucleus and tract in the pons. Facial diplegia is an extremely rare condition that occurs in approximately 0.3% to 2.0% of all facial palsies. Electrodiagnostic studies including direct facial nerve conduction, facial electromyography (EMG), and blink reflex studies are useful for the prognosis and lesion localization in facial nerve palsy.MethodologyThis retrospective, observational study was conducted at the Neurophysiology Unit, Hamad General Hospital, Doha, Qatar. This study included 11 patients with bilateral facial weakness who visited for electrodiagnostic studies in the neurophysiology laboratory.ResultsIn total, eight (72.7%) patients had facial diplegia, eight (72.7%) had hypo/areflexia, seven (63.6%) had facial numbness, and five (45.5%) had cerebrospinal fluid albuminocytological dissociation. The most frequent cause of facial diplegia in this study was GBS (81.9%). Direct facial nerve conduction stimulation showed that nine (81.8%) patients had bilateral facial nerve low compound muscle action potential amplitudes. The bilateral blink reflex study showed that eight (88.8%) patients had absent bilateral evoked responses. Finally, the EMG study showed that five (55.5%) patients had active denervation in bilateral sample facial muscles.ConclusionsBilateral facial nerve palsy is an extremely rare condition with a varied etiology. Electrodiagnostic studies are useful in detecting the underlying pathophysiologic processes, prognosis, and central or peripheral lesion localization in patients with facial diplegia.</description><subject>Ataxia</subject><subject>Diagnostic tests</subject><subject>Dysarthria</subject><subject>Dysphagia</subject><subject>Electromyography</subject><subject>Guillain-Barre syndrome</subject><subject>Internal Medicine</subject><subject>Lyme disease</subject><subject>Medical prognosis</subject><subject>Neurological disorders</subject><subject>Neurology</subject><subject>Neurophysiology</subject><subject>Proteins</subject><subject>Viral infections</subject><issn>2168-8184</issn><issn>2168-8184</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><recordid>eNpdkU1v1DAQhiMEolXpjR9giQsHUmzHX-GAVEpbkFYCUcrVmjiTZaqsvdgJUnvhrzfLVgg4zdejVzPzVtVzwU-s1e3rMGecy4nUXNlH1aEUxtVOOPX4r_ygOi7lhnMuuJXc8qfVQaOtaG2rD6tfKyyUIlulACPdwbQrIPbsc07rmAoVdl0ortn5iGHKqSfYtScK7Gqae8LCKLILCAQje0_bEdcEb9gp-wIZ2TfIBHFiaWCXM40jUKzfQV4mV7exz2mDz6onA4wFjx_iUXV9cf717EO9-nT58ex0VQdpzVQbOWijewDVobFGq05pJ5QCqwQ0rtNdi4iudw4ABwwSBm4QZNe1BgczNEfV273udu422AeMU4bRbzNtIN_6BOT_nUT67tfpp2_l7nHtIvDyQSCnHzOWyW-oBFxuipjm4qWxzirdSLWgL_5Db9Kc43LeQjlptDZCLtSrPRVyKiXj8GcZwf3OXL831_82t7kH28GaDw</recordid><startdate>20220516</startdate><enddate>20220516</enddate><creator>Ali, Liaquat</creator><creator>Alhatou, Mohammed</creator><creator>Adeli, Gholam</creator><creator>Elalamy, Osama</creator><creator>Zada, Yasin</creator><creator>Mohammed, Imran</creator><creator>Sharif, Muhammad</creator><creator>Noor Illahi, Memon</creator><creator>Naeem, Muhammad</creator><creator>Iqrar, Ambreen</creator><general>Cureus Inc</general><general>Cureus</general><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>COVID</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20220516</creationdate><title>Lesion Localization and Prognosis Using Electrodiagnostic Studies in Facial Diplegia: A Rare Variant of Guillain-Barre Syndrome</title><author>Ali, Liaquat ; Alhatou, Mohammed ; Adeli, Gholam ; Elalamy, Osama ; Zada, Yasin ; Mohammed, Imran ; Sharif, Muhammad ; Noor Illahi, Memon ; Naeem, Muhammad ; Iqrar, Ambreen</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c276t-62f565daa4be67654b458144a741a38b5b9eee8d88aaefec2af06ea2bb96ef6f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Ataxia</topic><topic>Diagnostic tests</topic><topic>Dysarthria</topic><topic>Dysphagia</topic><topic>Electromyography</topic><topic>Guillain-Barre syndrome</topic><topic>Internal Medicine</topic><topic>Lyme disease</topic><topic>Medical prognosis</topic><topic>Neurological disorders</topic><topic>Neurology</topic><topic>Neurophysiology</topic><topic>Proteins</topic><topic>Viral infections</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ali, Liaquat</creatorcontrib><creatorcontrib>Alhatou, Mohammed</creatorcontrib><creatorcontrib>Adeli, Gholam</creatorcontrib><creatorcontrib>Elalamy, Osama</creatorcontrib><creatorcontrib>Zada, Yasin</creatorcontrib><creatorcontrib>Mohammed, Imran</creatorcontrib><creatorcontrib>Sharif, Muhammad</creatorcontrib><creatorcontrib>Noor Illahi, Memon</creatorcontrib><creatorcontrib>Naeem, Muhammad</creatorcontrib><creatorcontrib>Iqrar, Ambreen</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Coronavirus Research Database</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Curēus (Palo Alto, CA)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ali, Liaquat</au><au>Alhatou, Mohammed</au><au>Adeli, Gholam</au><au>Elalamy, Osama</au><au>Zada, Yasin</au><au>Mohammed, Imran</au><au>Sharif, Muhammad</au><au>Noor Illahi, Memon</au><au>Naeem, Muhammad</au><au>Iqrar, Ambreen</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Lesion Localization and Prognosis Using Electrodiagnostic Studies in Facial Diplegia: A Rare Variant of Guillain-Barre Syndrome</atitle><jtitle>Curēus (Palo Alto, CA)</jtitle><date>2022-05-16</date><risdate>2022</risdate><volume>14</volume><issue>5</issue><spage>e25047</spage><epage>e25047</epage><pages>e25047-e25047</pages><issn>2168-8184</issn><eissn>2168-8184</eissn><abstract>BackgroundThe etiology of facial nerve palsy is diverse and includes herpes zoster virus, Guillain-Barre syndrome (GBS), otitis media, Lyme disease, sarcoidosis, human immunodeficiency virus, etc. The lower motor neuron type facial nerve palsy is usually caused by an ipsilateral facial nerve lesion; however, it may be caused by a central lesion of the facial nerve nucleus and tract in the pons. Facial diplegia is an extremely rare condition that occurs in approximately 0.3% to 2.0% of all facial palsies. Electrodiagnostic studies including direct facial nerve conduction, facial electromyography (EMG), and blink reflex studies are useful for the prognosis and lesion localization in facial nerve palsy.MethodologyThis retrospective, observational study was conducted at the Neurophysiology Unit, Hamad General Hospital, Doha, Qatar. This study included 11 patients with bilateral facial weakness who visited for electrodiagnostic studies in the neurophysiology laboratory.ResultsIn total, eight (72.7%) patients had facial diplegia, eight (72.7%) had hypo/areflexia, seven (63.6%) had facial numbness, and five (45.5%) had cerebrospinal fluid albuminocytological dissociation. The most frequent cause of facial diplegia in this study was GBS (81.9%). Direct facial nerve conduction stimulation showed that nine (81.8%) patients had bilateral facial nerve low compound muscle action potential amplitudes. The bilateral blink reflex study showed that eight (88.8%) patients had absent bilateral evoked responses. Finally, the EMG study showed that five (55.5%) patients had active denervation in bilateral sample facial muscles.ConclusionsBilateral facial nerve palsy is an extremely rare condition with a varied etiology. Electrodiagnostic studies are useful in detecting the underlying pathophysiologic processes, prognosis, and central or peripheral lesion localization in patients with facial diplegia.</abstract><cop>Palo Alto</cop><pub>Cureus Inc</pub><pmid>35719795</pmid><doi>10.7759/cureus.25047</doi><oa>free_for_read</oa></addata></record> |
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subjects | Ataxia Diagnostic tests Dysarthria Dysphagia Electromyography Guillain-Barre syndrome Internal Medicine Lyme disease Medical prognosis Neurological disorders Neurology Neurophysiology Proteins Viral infections |
title | Lesion Localization and Prognosis Using Electrodiagnostic Studies in Facial Diplegia: A Rare Variant of Guillain-Barre Syndrome |
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