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Mitochondrial 3243 A→G mutation (MELAS mutation) associated with painful muscle stiffness
The mitochondrial mutation A→G at nucleotide position 3243 is associated with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS) and other mitochondrial encephalomyopathies. We found this mutation in a 61-year-old patient who developed at the age of 54 a myopath...
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Published in: | Neuromuscular disorders : NMD 1999-07, Vol.9 (5), p.305-307 |
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creator | Deschauer, M. Wieser, T. Neudecker, S. Lindner, A. Zierz, S. |
description | The mitochondrial mutation A→G at nucleotide position 3243 is associated with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS) and other mitochondrial encephalomyopathies. We found this mutation in a 61-year-old patient who developed at the age of 54 a myopathy with painful muscle stiffness as the predominant symptom. Additionally hypacusis, a mild hemisensory syndrome and impaired glucose tolerance were present. Muscle histopathology showed few ragged red fibers. The mutation was detected heteroplasmatically in DNA from muscle and blood. So far painful muscle stiffness has not been a known phenotype of the 3243 mutation. |
doi_str_mv | 10.1016/S0960-8966(99)00019-X |
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We found this mutation in a 61-year-old patient who developed at the age of 54 a myopathy with painful muscle stiffness as the predominant symptom. Additionally hypacusis, a mild hemisensory syndrome and impaired glucose tolerance were present. Muscle histopathology showed few ragged red fibers. The mutation was detected heteroplasmatically in DNA from muscle and blood. So far painful muscle stiffness has not been a known phenotype of the 3243 mutation.</description><identifier>ISSN: 0960-8966</identifier><identifier>EISSN: 1873-2364</identifier><identifier>DOI: 10.1016/S0960-8966(99)00019-X</identifier><identifier>PMID: 10407850</identifier><language>eng</language><publisher>England: Elsevier B.V</publisher><subject>DNA, Mitochondrial - genetics ; Humans ; Male ; MELAS ; Middle Aged ; Mitochondria, Muscle - genetics ; Mitochondrial mutation ; Muscle Weakness - complications ; Muscle Weakness - genetics ; Muscle Weakness - pathology ; Muscle, Skeletal - metabolism ; Muscle, Skeletal - pathology ; Muscular Diseases - complications ; Muscular Diseases - genetics ; Muscular Diseases - pathology ; Pain - etiology ; Painful muscle stiffness ; Point Mutation</subject><ispartof>Neuromuscular disorders : NMD, 1999-07, Vol.9 (5), p.305-307</ispartof><rights>1999 Elsevier Science B.V.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c361t-46e7d6f0e9453b0a56b4eb9b077154848fde16cf6625963a5a2fc8d676985bb33</citedby><cites>FETCH-LOGICAL-c361t-46e7d6f0e9453b0a56b4eb9b077154848fde16cf6625963a5a2fc8d676985bb33</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/10407850$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Deschauer, M.</creatorcontrib><creatorcontrib>Wieser, T.</creatorcontrib><creatorcontrib>Neudecker, S.</creatorcontrib><creatorcontrib>Lindner, A.</creatorcontrib><creatorcontrib>Zierz, S.</creatorcontrib><title>Mitochondrial 3243 A→G mutation (MELAS mutation) associated with painful muscle stiffness</title><title>Neuromuscular disorders : NMD</title><addtitle>Neuromuscul Disord</addtitle><description>The mitochondrial mutation A→G at nucleotide position 3243 is associated with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS) and other mitochondrial encephalomyopathies. We found this mutation in a 61-year-old patient who developed at the age of 54 a myopathy with painful muscle stiffness as the predominant symptom. Additionally hypacusis, a mild hemisensory syndrome and impaired glucose tolerance were present. Muscle histopathology showed few ragged red fibers. The mutation was detected heteroplasmatically in DNA from muscle and blood. So far painful muscle stiffness has not been a known phenotype of the 3243 mutation.</description><subject>DNA, Mitochondrial - genetics</subject><subject>Humans</subject><subject>Male</subject><subject>MELAS</subject><subject>Middle Aged</subject><subject>Mitochondria, Muscle - genetics</subject><subject>Mitochondrial mutation</subject><subject>Muscle Weakness - complications</subject><subject>Muscle Weakness - genetics</subject><subject>Muscle Weakness - pathology</subject><subject>Muscle, Skeletal - metabolism</subject><subject>Muscle, Skeletal - pathology</subject><subject>Muscular Diseases - complications</subject><subject>Muscular Diseases - genetics</subject><subject>Muscular Diseases - pathology</subject><subject>Pain - etiology</subject><subject>Painful muscle stiffness</subject><subject>Point Mutation</subject><issn>0960-8966</issn><issn>1873-2364</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><recordid>eNqFkMtKxDAUhoMoOo4-gtKV6KKaNJc2KxlkvMCIi1EQXIQ0PcFIL2OTKr6AD-Aj-iR2pjK4c3U48P3n53wIHRB8SjARZ3MsBY4zKcSxlCcYYyLjxw00IllK44QKtolGa2QH7Xr_0jM8Fek22iGY4TTjeISebl1ozHNTF63TZUQTRqPJ9-fXVVR1QQfX1NHx7XQ2ma_3k0h73xinAxTRuwvP0UK72nZlT3hTQuSDs7YG7_fQltWlh_3fOUYPl9P7i-t4dnd1czGZxYYKEmImIC2ExSAZpznWXOQMcpnjNCWcZSyzBRBhrBAJl4JqrhNrskKkQmY8zykdo6Ph7qJtXjvwQVXOGyhLXUPTedVzMiEM9yAfQNM23rdg1aJ1lW4_FMFqaVWtrKqlMiWlWllVj33u8Legyyso_qQGjT1wPgDQv_nmoFXeOKgNFK4FE1TRuH8qfgAXaIeC</recordid><startdate>19990701</startdate><enddate>19990701</enddate><creator>Deschauer, M.</creator><creator>Wieser, T.</creator><creator>Neudecker, S.</creator><creator>Lindner, A.</creator><creator>Zierz, S.</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></search><sort><creationdate>19990701</creationdate><title>Mitochondrial 3243 A→G mutation (MELAS mutation) associated with painful muscle stiffness</title><author>Deschauer, M. ; Wieser, T. ; Neudecker, S. ; Lindner, A. ; Zierz, S.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c361t-46e7d6f0e9453b0a56b4eb9b077154848fde16cf6625963a5a2fc8d676985bb33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>DNA, Mitochondrial - genetics</topic><topic>Humans</topic><topic>Male</topic><topic>MELAS</topic><topic>Middle Aged</topic><topic>Mitochondria, Muscle - genetics</topic><topic>Mitochondrial mutation</topic><topic>Muscle Weakness - complications</topic><topic>Muscle Weakness - genetics</topic><topic>Muscle Weakness - pathology</topic><topic>Muscle, Skeletal - metabolism</topic><topic>Muscle, Skeletal - pathology</topic><topic>Muscular Diseases - complications</topic><topic>Muscular Diseases - genetics</topic><topic>Muscular Diseases - pathology</topic><topic>Pain - etiology</topic><topic>Painful muscle stiffness</topic><topic>Point Mutation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Deschauer, M.</creatorcontrib><creatorcontrib>Wieser, T.</creatorcontrib><creatorcontrib>Neudecker, S.</creatorcontrib><creatorcontrib>Lindner, A.</creatorcontrib><creatorcontrib>Zierz, S.</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><jtitle>Neuromuscular disorders : NMD</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Deschauer, M.</au><au>Wieser, T.</au><au>Neudecker, S.</au><au>Lindner, A.</au><au>Zierz, S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Mitochondrial 3243 A→G mutation (MELAS mutation) associated with painful muscle stiffness</atitle><jtitle>Neuromuscular disorders : NMD</jtitle><addtitle>Neuromuscul Disord</addtitle><date>1999-07-01</date><risdate>1999</risdate><volume>9</volume><issue>5</issue><spage>305</spage><epage>307</epage><pages>305-307</pages><issn>0960-8966</issn><eissn>1873-2364</eissn><abstract>The mitochondrial mutation A→G at nucleotide position 3243 is associated with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS) and other mitochondrial encephalomyopathies. We found this mutation in a 61-year-old patient who developed at the age of 54 a myopathy with painful muscle stiffness as the predominant symptom. Additionally hypacusis, a mild hemisensory syndrome and impaired glucose tolerance were present. Muscle histopathology showed few ragged red fibers. The mutation was detected heteroplasmatically in DNA from muscle and blood. So far painful muscle stiffness has not been a known phenotype of the 3243 mutation.</abstract><cop>England</cop><pub>Elsevier B.V</pub><pmid>10407850</pmid><doi>10.1016/S0960-8966(99)00019-X</doi><tpages>3</tpages></addata></record> |
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source | ScienceDirect Journals |
subjects | DNA, Mitochondrial - genetics Humans Male MELAS Middle Aged Mitochondria, Muscle - genetics Mitochondrial mutation Muscle Weakness - complications Muscle Weakness - genetics Muscle Weakness - pathology Muscle, Skeletal - metabolism Muscle, Skeletal - pathology Muscular Diseases - complications Muscular Diseases - genetics Muscular Diseases - pathology Pain - etiology Painful muscle stiffness Point Mutation |
title | Mitochondrial 3243 A→G mutation (MELAS mutation) associated with painful muscle stiffness |
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