Apraxia of speech and cerebellar mutism syndrome: a case report
Cerebellar mutism syndrome (CMS) or posterior fossa syndrome (PFS) consists of a constellation of neuropsychiatric, neuropsychological and neurogenic speech and language deficits. It is most commonly observed in children after posterior fossa tumor surgery. The most prominent feature of CMS is mutis...
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description | Cerebellar mutism syndrome (CMS) or posterior fossa syndrome (PFS) consists of a constellation of neuropsychiatric, neuropsychological and neurogenic speech and language deficits. It is most commonly observed in children after posterior fossa tumor surgery. The most prominent feature of CMS is mutism, which generally starts after a few days after the operation, has a limited duration and is typically followed by motor speech deficits. However, the core speech disorder subserving CMS is still unclear.
This study investigates the speech and language symptoms following posterior fossa medulloblastoma surgery in a 12-year-old right-handed boy. An extensive battery of formal speech (DIAS = Diagnostic Instrument Apraxia of Speech) and language tests were administered during a follow-up of 6 weeks after surgery. Although the neurological and neuropsychological (affective, cognitive) symptoms of this patient are consistent with Schmahmann's syndrome, the speech and language symptoms were markedly different from what is typically described in the literature. In-depth analyses of speech production revealed features consistent with a diagnosis of apraxia of speech (AoS) while ataxic dysarthria was completely absent. In addition, language assessments showed genuine aphasic deficits as reflected by distorted language production and perception, wordfinding difficulties, grammatical disturbances and verbal fluency deficits.
To the best of our knowledge this case might be the first example that clearly demonstrates that a higher level motor planning disorder (apraxia) may be the origin of disrupted speech in CMS. In addition, identification of non-motor linguistic disturbances during follow-up add to the view that the cerebellum not only plays a crucial role in the planning and execution of speech but also in linguistic processing. Whether the cerebellum has a direct or indirect role in motor speech planning needs to be further investigated. |
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This study investigates the speech and language symptoms following posterior fossa medulloblastoma surgery in a 12-year-old right-handed boy. An extensive battery of formal speech (DIAS = Diagnostic Instrument Apraxia of Speech) and language tests were administered during a follow-up of 6 weeks after surgery. Although the neurological and neuropsychological (affective, cognitive) symptoms of this patient are consistent with Schmahmann's syndrome, the speech and language symptoms were markedly different from what is typically described in the literature. In-depth analyses of speech production revealed features consistent with a diagnosis of apraxia of speech (AoS) while ataxic dysarthria was completely absent. In addition, language assessments showed genuine aphasic deficits as reflected by distorted language production and perception, wordfinding difficulties, grammatical disturbances and verbal fluency deficits.
To the best of our knowledge this case might be the first example that clearly demonstrates that a higher level motor planning disorder (apraxia) may be the origin of disrupted speech in CMS. In addition, identification of non-motor linguistic disturbances during follow-up add to the view that the cerebellum not only plays a crucial role in the planning and execution of speech but also in linguistic processing. Whether the cerebellum has a direct or indirect role in motor speech planning needs to be further investigated.</description><identifier>ISSN: 2053-8871</identifier><identifier>EISSN: 2053-8871</identifier><identifier>DOI: 10.1186/s40673-016-0059-x</identifier><identifier>PMID: 28074148</identifier><language>eng</language><publisher>England: BioMed Central</publisher><subject>Case Report</subject><ispartof>Cerebellum & ataxias, 2017-01, Vol.4 (1), p.2, Article 2</ispartof><rights>Copyright BioMed Central 2017</rights><rights>The Author(s). 2017</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c309x-70f4cb45523321a7529ef6c995ce746b1c930c6a9e31a2518821d6d19666ee7e3</citedby><cites>FETCH-LOGICAL-c309x-70f4cb45523321a7529ef6c995ce746b1c930c6a9e31a2518821d6d19666ee7e3</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/PMC5217307/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5217307/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28074148$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>De Witte, E</creatorcontrib><creatorcontrib>Wilssens, I</creatorcontrib><creatorcontrib>De Surgeloose, D</creatorcontrib><creatorcontrib>Dua, G</creatorcontrib><creatorcontrib>Moens, M</creatorcontrib><creatorcontrib>Verhoeven, J</creatorcontrib><creatorcontrib>Manto, M</creatorcontrib><creatorcontrib>Mariën, P</creatorcontrib><title>Apraxia of speech and cerebellar mutism syndrome: a case report</title><title>Cerebellum & ataxias</title><addtitle>Cerebellum Ataxias</addtitle><description>Cerebellar mutism syndrome (CMS) or posterior fossa syndrome (PFS) consists of a constellation of neuropsychiatric, neuropsychological and neurogenic speech and language deficits. It is most commonly observed in children after posterior fossa tumor surgery. The most prominent feature of CMS is mutism, which generally starts after a few days after the operation, has a limited duration and is typically followed by motor speech deficits. However, the core speech disorder subserving CMS is still unclear.
This study investigates the speech and language symptoms following posterior fossa medulloblastoma surgery in a 12-year-old right-handed boy. An extensive battery of formal speech (DIAS = Diagnostic Instrument Apraxia of Speech) and language tests were administered during a follow-up of 6 weeks after surgery. Although the neurological and neuropsychological (affective, cognitive) symptoms of this patient are consistent with Schmahmann's syndrome, the speech and language symptoms were markedly different from what is typically described in the literature. In-depth analyses of speech production revealed features consistent with a diagnosis of apraxia of speech (AoS) while ataxic dysarthria was completely absent. In addition, language assessments showed genuine aphasic deficits as reflected by distorted language production and perception, wordfinding difficulties, grammatical disturbances and verbal fluency deficits.
To the best of our knowledge this case might be the first example that clearly demonstrates that a higher level motor planning disorder (apraxia) may be the origin of disrupted speech in CMS. In addition, identification of non-motor linguistic disturbances during follow-up add to the view that the cerebellum not only plays a crucial role in the planning and execution of speech but also in linguistic processing. Whether the cerebellum has a direct or indirect role in motor speech planning needs to be further investigated.</description><subject>Case Report</subject><issn>2053-8871</issn><issn>2053-8871</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>BENPR</sourceid><recordid>eNpVkEtLAzEUhYMottT-ADcScD2axySZuFBK8QUFN7oOmcwdO2VeJjMy_fdOaZW6uhfuOecePoQuKbmhNJG3ISZS8YhQGREidDScoCkjgkdJoujp0T5B8xA2hBDKhGZMn6MJS4iKaZxM0cOi9XYoLG5yHFoAt8a2zrADDymUpfW46rsiVDhs68w3Fdxhi50NgD20je8u0FluywDzw5yhj6fH9-VLtHp7fl0uVpHjRA-RInns0lgIxjmjVgmmIZdOa-FAxTKlTnPipNXAqWWCJgmjmcyollICKOAzdL_Pbfu0gsxB3XlbmtYXlfVb09jC_L_Uxdp8Nt9GMKo4UWPA9SHAN189hM5smt7XY2cz0owTMdLZqehe5XwTgof87wMlZofd7LGbEbvZYTfD6Lk6rvbn-IXMfwC8A31W</recordid><startdate>20170106</startdate><enddate>20170106</enddate><creator>De Witte, E</creator><creator>Wilssens, I</creator><creator>De Surgeloose, D</creator><creator>Dua, G</creator><creator>Moens, M</creator><creator>Verhoeven, J</creator><creator>Manto, M</creator><creator>Mariën, P</creator><general>BioMed Central</general><scope>NPM</scope><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>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>PHGZM</scope><scope>PHGZT</scope><scope>PIMPY</scope><scope>PKEHL</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>5PM</scope></search><sort><creationdate>20170106</creationdate><title>Apraxia of speech and cerebellar mutism syndrome: a case report</title><author>De Witte, E ; Wilssens, I ; De Surgeloose, D ; Dua, G ; Moens, M ; Verhoeven, J ; Manto, M ; Mariën, P</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c309x-70f4cb45523321a7529ef6c995ce746b1c930c6a9e31a2518821d6d19666ee7e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Case Report</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>De Witte, E</creatorcontrib><creatorcontrib>Wilssens, I</creatorcontrib><creatorcontrib>De Surgeloose, D</creatorcontrib><creatorcontrib>Dua, G</creatorcontrib><creatorcontrib>Moens, M</creatorcontrib><creatorcontrib>Verhoeven, J</creatorcontrib><creatorcontrib>Manto, M</creatorcontrib><creatorcontrib>Mariën, P</creatorcontrib><collection>PubMed</collection><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>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>ProQuest Central (New)</collection><collection>ProQuest One Academic (New)</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Middle East (New)</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>PubMed Central (Full Participant titles)</collection><jtitle>Cerebellum & ataxias</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>De Witte, E</au><au>Wilssens, I</au><au>De Surgeloose, D</au><au>Dua, G</au><au>Moens, M</au><au>Verhoeven, J</au><au>Manto, M</au><au>Mariën, P</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Apraxia of speech and cerebellar mutism syndrome: a case report</atitle><jtitle>Cerebellum & ataxias</jtitle><addtitle>Cerebellum Ataxias</addtitle><date>2017-01-06</date><risdate>2017</risdate><volume>4</volume><issue>1</issue><spage>2</spage><pages>2-</pages><artnum>2</artnum><issn>2053-8871</issn><eissn>2053-8871</eissn><abstract>Cerebellar mutism syndrome (CMS) or posterior fossa syndrome (PFS) consists of a constellation of neuropsychiatric, neuropsychological and neurogenic speech and language deficits. It is most commonly observed in children after posterior fossa tumor surgery. The most prominent feature of CMS is mutism, which generally starts after a few days after the operation, has a limited duration and is typically followed by motor speech deficits. However, the core speech disorder subserving CMS is still unclear.
This study investigates the speech and language symptoms following posterior fossa medulloblastoma surgery in a 12-year-old right-handed boy. An extensive battery of formal speech (DIAS = Diagnostic Instrument Apraxia of Speech) and language tests were administered during a follow-up of 6 weeks after surgery. Although the neurological and neuropsychological (affective, cognitive) symptoms of this patient are consistent with Schmahmann's syndrome, the speech and language symptoms were markedly different from what is typically described in the literature. In-depth analyses of speech production revealed features consistent with a diagnosis of apraxia of speech (AoS) while ataxic dysarthria was completely absent. In addition, language assessments showed genuine aphasic deficits as reflected by distorted language production and perception, wordfinding difficulties, grammatical disturbances and verbal fluency deficits.
To the best of our knowledge this case might be the first example that clearly demonstrates that a higher level motor planning disorder (apraxia) may be the origin of disrupted speech in CMS. In addition, identification of non-motor linguistic disturbances during follow-up add to the view that the cerebellum not only plays a crucial role in the planning and execution of speech but also in linguistic processing. Whether the cerebellum has a direct or indirect role in motor speech planning needs to be further investigated.</abstract><cop>England</cop><pub>BioMed Central</pub><pmid>28074148</pmid><doi>10.1186/s40673-016-0059-x</doi><oa>free_for_read</oa></addata></record> |
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title | Apraxia of speech and cerebellar mutism syndrome: a case report |
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