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Dysphagia is present but mild in myotonic dystrophy type 2
Abstract The phenotype of myotonic dystrophy type 2 (DM2) shows similarities as well as differences to that of myotonic dystrophy type 1 (DM1). Dysphagia, a predominant feature in DM1, has not yet been examined in DM2. In a recent nationwide questionnaire survey of gastrointestinal symptoms in DM2,...
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Published in: | Neuromuscular disorders : NMD 2009-03, Vol.19 (3), p.196-198 |
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container_title | Neuromuscular disorders : NMD |
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creator | Tieleman, A.A Knuijt, S van Vliet, J de Swart, B.J.M Ensink, R van Engelen, B.G.M |
description | Abstract The phenotype of myotonic dystrophy type 2 (DM2) shows similarities as well as differences to that of myotonic dystrophy type 1 (DM1). Dysphagia, a predominant feature in DM1, has not yet been examined in DM2. In a recent nationwide questionnaire survey of gastrointestinal symptoms in DM2, 12 out of 29 DM2 patients reported to have difficulty in swallowing for solid food. The aim of the study was to investigate the presence of dysphagia in patients with genetically proven DM2 who reported difficulty in swallowing for solid food at the questionnaire survey. Swallowing function and fiberoptic endoscopic evaluation of swallowing (FEES) were examined by a speech therapist and otorhinolaryngologist, respectively. In DM2 patients who reported difficulty in swallowing the presence of dysphagia could be confirmed (clinically in 100%, by FEES in 88%). A correlation exists between Dysphagia Outcome and Severity Score (DOSS) and age ( p = 0.05). None of the patients was underweight, and none of the patients had suffered aspiration pneumonia in the past. Dysphagia is present among DM2 patients and is more severe in older patients. However, dysphagia is generally mild, and do not lead to weight loss, or aspiration pneumonia. |
doi_str_mv | 10.1016/j.nmd.2008.12.002 |
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Dysphagia, a predominant feature in DM1, has not yet been examined in DM2. In a recent nationwide questionnaire survey of gastrointestinal symptoms in DM2, 12 out of 29 DM2 patients reported to have difficulty in swallowing for solid food. The aim of the study was to investigate the presence of dysphagia in patients with genetically proven DM2 who reported difficulty in swallowing for solid food at the questionnaire survey. Swallowing function and fiberoptic endoscopic evaluation of swallowing (FEES) were examined by a speech therapist and otorhinolaryngologist, respectively. In DM2 patients who reported difficulty in swallowing the presence of dysphagia could be confirmed (clinically in 100%, by FEES in 88%). A correlation exists between Dysphagia Outcome and Severity Score (DOSS) and age ( p = 0.05). None of the patients was underweight, and none of the patients had suffered aspiration pneumonia in the past. Dysphagia is present among DM2 patients and is more severe in older patients. However, dysphagia is generally mild, and do not lead to weight loss, or aspiration pneumonia.</description><identifier>ISSN: 0960-8966</identifier><identifier>EISSN: 1873-2364</identifier><identifier>DOI: 10.1016/j.nmd.2008.12.002</identifier><identifier>PMID: 19167224</identifier><language>eng</language><publisher>England: Elsevier B.V</publisher><subject>Adult ; Age Distribution ; Aged ; Data Collection ; Deglutition - physiology ; Deglutition Disorders - diagnosis ; Deglutition Disorders - genetics ; Deglutition Disorders - physiopathology ; Disability Evaluation ; Dysphagia ; Endoscopy, Gastrointestinal ; Esophagus - physiopathology ; Female ; Fiberoptic endoscopic evaluation of swallowing (FEES) ; Genetic Predisposition to Disease - genetics ; Humans ; Male ; Middle Aged ; Muscle, Skeletal - physiopathology ; Myotonic Dystrophy - classification ; Myotonic Dystrophy - complications ; Myotonic Dystrophy - physiopathology ; Myotonic dystrophy type 2 ; Neurology ; Pharynx - physiopathology ; PROMM ; Severity of Illness Index ; Surveys and Questionnaires ; Swallowing difficulty</subject><ispartof>Neuromuscular disorders : NMD, 2009-03, Vol.19 (3), p.196-198</ispartof><rights>2009</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c438t-8340c6bba724b6f19e0dc77d535e702b700087389273b338b5a10184e081ff063</citedby><cites>FETCH-LOGICAL-c438t-8340c6bba724b6f19e0dc77d535e702b700087389273b338b5a10184e081ff063</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19167224$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tieleman, A.A</creatorcontrib><creatorcontrib>Knuijt, S</creatorcontrib><creatorcontrib>van Vliet, J</creatorcontrib><creatorcontrib>de Swart, B.J.M</creatorcontrib><creatorcontrib>Ensink, R</creatorcontrib><creatorcontrib>van Engelen, B.G.M</creatorcontrib><title>Dysphagia is present but mild in myotonic dystrophy type 2</title><title>Neuromuscular disorders : NMD</title><addtitle>Neuromuscul Disord</addtitle><description>Abstract The phenotype of myotonic dystrophy type 2 (DM2) shows similarities as well as differences to that of myotonic dystrophy type 1 (DM1). Dysphagia, a predominant feature in DM1, has not yet been examined in DM2. In a recent nationwide questionnaire survey of gastrointestinal symptoms in DM2, 12 out of 29 DM2 patients reported to have difficulty in swallowing for solid food. The aim of the study was to investigate the presence of dysphagia in patients with genetically proven DM2 who reported difficulty in swallowing for solid food at the questionnaire survey. Swallowing function and fiberoptic endoscopic evaluation of swallowing (FEES) were examined by a speech therapist and otorhinolaryngologist, respectively. In DM2 patients who reported difficulty in swallowing the presence of dysphagia could be confirmed (clinically in 100%, by FEES in 88%). A correlation exists between Dysphagia Outcome and Severity Score (DOSS) and age ( p = 0.05). None of the patients was underweight, and none of the patients had suffered aspiration pneumonia in the past. Dysphagia is present among DM2 patients and is more severe in older patients. However, dysphagia is generally mild, and do not lead to weight loss, or aspiration pneumonia.</description><subject>Adult</subject><subject>Age Distribution</subject><subject>Aged</subject><subject>Data Collection</subject><subject>Deglutition - physiology</subject><subject>Deglutition Disorders - diagnosis</subject><subject>Deglutition Disorders - genetics</subject><subject>Deglutition Disorders - physiopathology</subject><subject>Disability Evaluation</subject><subject>Dysphagia</subject><subject>Endoscopy, Gastrointestinal</subject><subject>Esophagus - physiopathology</subject><subject>Female</subject><subject>Fiberoptic endoscopic evaluation of swallowing (FEES)</subject><subject>Genetic Predisposition to Disease - genetics</subject><subject>Humans</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Muscle, Skeletal - physiopathology</subject><subject>Myotonic Dystrophy - classification</subject><subject>Myotonic Dystrophy - complications</subject><subject>Myotonic Dystrophy - physiopathology</subject><subject>Myotonic dystrophy type 2</subject><subject>Neurology</subject><subject>Pharynx - physiopathology</subject><subject>PROMM</subject><subject>Severity of Illness Index</subject><subject>Surveys and Questionnaires</subject><subject>Swallowing difficulty</subject><issn>0960-8966</issn><issn>1873-2364</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><recordid>eNp9kU1r3DAQhkVp6G4-fkAvRaf2ZGck2ZKcQKAkbRMI5JDkLGx53NXWX5HsgP99tOxCIYec5vK8LzPPEPKVQcqAyfNt2nd1ygF0yngKwD-RNdNKJFzI7DNZQyEh0YWUK3IcwhaA5UqqL2TFCiYV59maXNwsYdyUf11JXaCjx4D9RKt5op1ra-p62i3DNPTO0noJkx_GzUKnZUTKT8lRU7YBzw7zhDz__vV0fZvcP_y5u_55n9hM6CnRIgMrq6pUPKtkwwqE2ipV5yJHBbxSEPdXQhdciUoIXeVlPE5nCJo1DUhxQn7se0c_vMwYJtO5YLFtyx6HORitc4h3iTyS3z8kpQJR5EJHkO1B64cQPDZm9K4r_WIYmJ1aszVRrdmpNYybqDZmvh3K56rD-n_i4DICl3sAo4xXh94E67C3WDuPdjL14D6sv3qXtq2L2sv2Hy4YtsPs-2jZMBNiwDzufrt7LWgAxZQSb3bpm9s</recordid><startdate>20090301</startdate><enddate>20090301</enddate><creator>Tieleman, A.A</creator><creator>Knuijt, S</creator><creator>van Vliet, J</creator><creator>de Swart, B.J.M</creator><creator>Ensink, R</creator><creator>van Engelen, B.G.M</creator><general>Elsevier B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>7TK</scope></search><sort><creationdate>20090301</creationdate><title>Dysphagia is present but mild in myotonic dystrophy type 2</title><author>Tieleman, A.A ; Knuijt, S ; van Vliet, J ; de Swart, B.J.M ; Ensink, R ; van Engelen, B.G.M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c438t-8340c6bba724b6f19e0dc77d535e702b700087389273b338b5a10184e081ff063</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Adult</topic><topic>Age Distribution</topic><topic>Aged</topic><topic>Data Collection</topic><topic>Deglutition - physiology</topic><topic>Deglutition Disorders - diagnosis</topic><topic>Deglutition Disorders - genetics</topic><topic>Deglutition Disorders - physiopathology</topic><topic>Disability Evaluation</topic><topic>Dysphagia</topic><topic>Endoscopy, Gastrointestinal</topic><topic>Esophagus - physiopathology</topic><topic>Female</topic><topic>Fiberoptic endoscopic evaluation of swallowing (FEES)</topic><topic>Genetic Predisposition to Disease - genetics</topic><topic>Humans</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Muscle, Skeletal - physiopathology</topic><topic>Myotonic Dystrophy - classification</topic><topic>Myotonic Dystrophy - complications</topic><topic>Myotonic Dystrophy - physiopathology</topic><topic>Myotonic dystrophy type 2</topic><topic>Neurology</topic><topic>Pharynx - physiopathology</topic><topic>PROMM</topic><topic>Severity of Illness Index</topic><topic>Surveys and Questionnaires</topic><topic>Swallowing difficulty</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tieleman, A.A</creatorcontrib><creatorcontrib>Knuijt, S</creatorcontrib><creatorcontrib>van Vliet, J</creatorcontrib><creatorcontrib>de Swart, B.J.M</creatorcontrib><creatorcontrib>Ensink, R</creatorcontrib><creatorcontrib>van Engelen, B.G.M</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Neurosciences Abstracts</collection><jtitle>Neuromuscular disorders : NMD</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tieleman, A.A</au><au>Knuijt, S</au><au>van Vliet, J</au><au>de Swart, B.J.M</au><au>Ensink, R</au><au>van Engelen, B.G.M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Dysphagia is present but mild in myotonic dystrophy type 2</atitle><jtitle>Neuromuscular disorders : NMD</jtitle><addtitle>Neuromuscul Disord</addtitle><date>2009-03-01</date><risdate>2009</risdate><volume>19</volume><issue>3</issue><spage>196</spage><epage>198</epage><pages>196-198</pages><issn>0960-8966</issn><eissn>1873-2364</eissn><abstract>Abstract The phenotype of myotonic dystrophy type 2 (DM2) shows similarities as well as differences to that of myotonic dystrophy type 1 (DM1). Dysphagia, a predominant feature in DM1, has not yet been examined in DM2. In a recent nationwide questionnaire survey of gastrointestinal symptoms in DM2, 12 out of 29 DM2 patients reported to have difficulty in swallowing for solid food. The aim of the study was to investigate the presence of dysphagia in patients with genetically proven DM2 who reported difficulty in swallowing for solid food at the questionnaire survey. Swallowing function and fiberoptic endoscopic evaluation of swallowing (FEES) were examined by a speech therapist and otorhinolaryngologist, respectively. In DM2 patients who reported difficulty in swallowing the presence of dysphagia could be confirmed (clinically in 100%, by FEES in 88%). A correlation exists between Dysphagia Outcome and Severity Score (DOSS) and age ( p = 0.05). None of the patients was underweight, and none of the patients had suffered aspiration pneumonia in the past. Dysphagia is present among DM2 patients and is more severe in older patients. However, dysphagia is generally mild, and do not lead to weight loss, or aspiration pneumonia.</abstract><cop>England</cop><pub>Elsevier B.V</pub><pmid>19167224</pmid><doi>10.1016/j.nmd.2008.12.002</doi><tpages>3</tpages></addata></record> |
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subjects | Adult Age Distribution Aged Data Collection Deglutition - physiology Deglutition Disorders - diagnosis Deglutition Disorders - genetics Deglutition Disorders - physiopathology Disability Evaluation Dysphagia Endoscopy, Gastrointestinal Esophagus - physiopathology Female Fiberoptic endoscopic evaluation of swallowing (FEES) Genetic Predisposition to Disease - genetics Humans Male Middle Aged Muscle, Skeletal - physiopathology Myotonic Dystrophy - classification Myotonic Dystrophy - complications Myotonic Dystrophy - physiopathology Myotonic dystrophy type 2 Neurology Pharynx - physiopathology PROMM Severity of Illness Index Surveys and Questionnaires Swallowing difficulty |
title | Dysphagia is present but mild in myotonic dystrophy type 2 |
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