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The unfolding spectrum of inherited distal myopathies
ABSTRACT Distal myopathies are a group of rare muscle diseases characterized by distal weakness at onset. Although acquired myopathies can occasionally present with distal weakness, the majority of distal myopathies have a genetic etiology. Their age of onset varies from early‐childhood to late‐adul...
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Published in: | Muscle & nerve 2019-03, Vol.59 (3), p.283-294 |
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Distal myopathies are a group of rare muscle diseases characterized by distal weakness at onset. Although acquired myopathies can occasionally present with distal weakness, the majority of distal myopathies have a genetic etiology. Their age of onset varies from early‐childhood to late‐adulthood while the predominant muscle weakness can affect calf, ankle dorsiflexor, or distal upper limb muscles. A spectrum of muscle pathological changes, varying from nonspecific myopathic changes to rimmed vacuoles to myofibrillar pathology to nuclei centralization, have been noted. Likewise, the underlying molecular defect is heterogeneous. In addition, there is emerging evidence that distal myopathies can result from defective proteins encoded by genes causative of neurogenic disorders, be manifestation of multisystem proteinopathies or the result of the altered interplay between different genes. In this review, we provide an overview on the clinical, electrophysiological, pathological, and molecular aspects of distal myopathies, focusing on the most recent developments in the field. Muscle Nerve 59:283–294, 2019 |
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Distal myopathies are a group of rare muscle diseases characterized by distal weakness at onset. Although acquired myopathies can occasionally present with distal weakness, the majority of distal myopathies have a genetic etiology. Their age of onset varies from early‐childhood to late‐adulthood while the predominant muscle weakness can affect calf, ankle dorsiflexor, or distal upper limb muscles. A spectrum of muscle pathological changes, varying from nonspecific myopathic changes to rimmed vacuoles to myofibrillar pathology to nuclei centralization, have been noted. Likewise, the underlying molecular defect is heterogeneous. In addition, there is emerging evidence that distal myopathies can result from defective proteins encoded by genes causative of neurogenic disorders, be manifestation of multisystem proteinopathies or the result of the altered interplay between different genes. In this review, we provide an overview on the clinical, electrophysiological, pathological, and molecular aspects of distal myopathies, focusing on the most recent developments in the field. Muscle Nerve 59:283–294, 2019</description><identifier>ISSN: 0148-639X</identifier><identifier>EISSN: 1097-4598</identifier><identifier>DOI: 10.1002/mus.26332</identifier><identifier>PMID: 30171629</identifier><language>eng</language><publisher>Hoboken, USA: John Wiley & Sons, Inc</publisher><subject>Ankle ; Children ; distal myopathy ; Etiology ; Genes ; multisystem proteinopathy ; Muscles ; myofibrillar myopathy ; neuromyopathy ; Proteins ; rimmed vacuoles ; Vacuoles</subject><ispartof>Muscle & nerve, 2019-03, Vol.59 (3), p.283-294</ispartof><rights>2018 Wiley Periodicals, Inc.</rights><rights>2019 Wiley Periodicals, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4192-3d915b9b71d696f59b25e640e252d7586822c73711839525d552b12154ab85453</citedby><cites>FETCH-LOGICAL-c4192-3d915b9b71d696f59b25e640e252d7586822c73711839525d552b12154ab85453</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30171629$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Milone, Margherita</creatorcontrib><creatorcontrib>Liewluck, Teerin</creatorcontrib><title>The unfolding spectrum of inherited distal myopathies</title><title>Muscle & nerve</title><addtitle>Muscle Nerve</addtitle><description>ABSTRACT
Distal myopathies are a group of rare muscle diseases characterized by distal weakness at onset. Although acquired myopathies can occasionally present with distal weakness, the majority of distal myopathies have a genetic etiology. Their age of onset varies from early‐childhood to late‐adulthood while the predominant muscle weakness can affect calf, ankle dorsiflexor, or distal upper limb muscles. A spectrum of muscle pathological changes, varying from nonspecific myopathic changes to rimmed vacuoles to myofibrillar pathology to nuclei centralization, have been noted. Likewise, the underlying molecular defect is heterogeneous. In addition, there is emerging evidence that distal myopathies can result from defective proteins encoded by genes causative of neurogenic disorders, be manifestation of multisystem proteinopathies or the result of the altered interplay between different genes. In this review, we provide an overview on the clinical, electrophysiological, pathological, and molecular aspects of distal myopathies, focusing on the most recent developments in the field. Muscle Nerve 59:283–294, 2019</description><subject>Ankle</subject><subject>Children</subject><subject>distal myopathy</subject><subject>Etiology</subject><subject>Genes</subject><subject>multisystem proteinopathy</subject><subject>Muscles</subject><subject>myofibrillar myopathy</subject><subject>neuromyopathy</subject><subject>Proteins</subject><subject>rimmed vacuoles</subject><subject>Vacuoles</subject><issn>0148-639X</issn><issn>1097-4598</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNp10M1LwzAYx_EgipvTg_-AFLzooVvypGmSowzfYOLBDbyFtkldRt9MWmT_vS2dHgRPz-XDl4cfQpcEzwnGsCg7P4eYUjhCU4IlDyMmxTGaYhKJMKbyfYLOvN9hjImI-SmaUEw4iUFOEVtvTdBVeV1oW30EvjFZ67oyqPPAVlvjbGt0oK1vkyIo93WTtFtr_Dk6yZPCm4vDnaHNw_16-RSuXh-fl3erMIuIhJBqSVgqU050LOOcyRSYiSNsgIHmTMQCIOOUEyKoZMA0Y5ASICxKUsEiRmfoZuw2rv7sjG9VaX1miiKpTN15BVgKzoEz6On1H7qrO1f13ykgAmhfgyF4O6rM1d47k6vG2TJxe0WwGrZU5ZAdtuzt1aHYpaXRv_JnvB4sRvBlC7P_v6ReNm9j8huPP3qP</recordid><startdate>201903</startdate><enddate>201903</enddate><creator>Milone, Margherita</creator><creator>Liewluck, Teerin</creator><general>John Wiley & Sons, Inc</general><general>Wiley Subscription Services, Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7T5</scope><scope>7TK</scope><scope>7TM</scope><scope>7TS</scope><scope>7U7</scope><scope>7U9</scope><scope>C1K</scope><scope>H94</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>7X8</scope></search><sort><creationdate>201903</creationdate><title>The unfolding spectrum of inherited distal myopathies</title><author>Milone, Margherita ; Liewluck, Teerin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4192-3d915b9b71d696f59b25e640e252d7586822c73711839525d552b12154ab85453</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Ankle</topic><topic>Children</topic><topic>distal myopathy</topic><topic>Etiology</topic><topic>Genes</topic><topic>multisystem proteinopathy</topic><topic>Muscles</topic><topic>myofibrillar myopathy</topic><topic>neuromyopathy</topic><topic>Proteins</topic><topic>rimmed vacuoles</topic><topic>Vacuoles</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Milone, Margherita</creatorcontrib><creatorcontrib>Liewluck, Teerin</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Physical Education Index</collection><collection>Toxicology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Premium</collection><collection>MEDLINE - Academic</collection><jtitle>Muscle & nerve</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Milone, Margherita</au><au>Liewluck, Teerin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The unfolding spectrum of inherited distal myopathies</atitle><jtitle>Muscle & nerve</jtitle><addtitle>Muscle Nerve</addtitle><date>2019-03</date><risdate>2019</risdate><volume>59</volume><issue>3</issue><spage>283</spage><epage>294</epage><pages>283-294</pages><issn>0148-639X</issn><eissn>1097-4598</eissn><abstract>ABSTRACT
Distal myopathies are a group of rare muscle diseases characterized by distal weakness at onset. Although acquired myopathies can occasionally present with distal weakness, the majority of distal myopathies have a genetic etiology. Their age of onset varies from early‐childhood to late‐adulthood while the predominant muscle weakness can affect calf, ankle dorsiflexor, or distal upper limb muscles. A spectrum of muscle pathological changes, varying from nonspecific myopathic changes to rimmed vacuoles to myofibrillar pathology to nuclei centralization, have been noted. Likewise, the underlying molecular defect is heterogeneous. In addition, there is emerging evidence that distal myopathies can result from defective proteins encoded by genes causative of neurogenic disorders, be manifestation of multisystem proteinopathies or the result of the altered interplay between different genes. In this review, we provide an overview on the clinical, electrophysiological, pathological, and molecular aspects of distal myopathies, focusing on the most recent developments in the field. Muscle Nerve 59:283–294, 2019</abstract><cop>Hoboken, USA</cop><pub>John Wiley & Sons, Inc</pub><pmid>30171629</pmid><doi>10.1002/mus.26332</doi><tpages>12</tpages></addata></record> |
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subjects | Ankle Children distal myopathy Etiology Genes multisystem proteinopathy Muscles myofibrillar myopathy neuromyopathy Proteins rimmed vacuoles Vacuoles |
title | The unfolding spectrum of inherited distal myopathies |
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