{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,9]],"date-time":"2026-10-09T02:02:20Z","timestamp":1791511340863,"version":"4.3.4"},"reference-count":17,"publisher":"SAGE Publications","license":[{"start":{"date-parts":[[2016,1,1]],"date-time":"2016-01-01T00:00:00Z","timestamp":1451606400000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/journals.sagepub.com\/page\/policies\/text-and-data-mining-license"}],"content-domain":{"domain":["journals.sagepub.com"],"crossmark-restriction":true},"short-container-title":["Child Neurology Open"],"published-print":{"date-parts":[[2016,1,1]]},"abstract":"<jats:p>Hereditary neuralgic amyotrophy is a rare disorder characterized by the sudden onset of recurrent episodes of painful brachial plexus neuropathies, followed by atrophy within a few weeks. The authors present the case of a 5-year-old boy who developed hereditary neuralgic amyotrophy in the right upper limb after a gastroenteritis illness. He made a full and rapid recovery with the use of intravenous immunoglobulin. A subsequent episode in the left upper limb during the course of intravenous immunoglobulin was significantly attenuated. A de novo c.262C&gt;T mutation in exon 2 of the SEPT9 gene was identified. To our knowledge, he is the first pediatric patient with SEPT9 hereditary neuralgic amyotrophy to be treated with intravenous immunoglobulin. The authors hypothesize that the c.262C&gt;T mutation in exon 2 of the SEPT9 gene generates pathology via the numerous isoforms under specific conditions and that intravenous immunoglobulin can play a role at the epigenetic level of improving dysfunctional SEPT9 expression.<\/jats:p>","DOI":"10.1177\/2329048x16668970","type":"journal-article","created":{"date-parts":[[2016,9,19]],"date-time":"2016-09-19T21:10:41Z","timestamp":1474319441000},"update-policy":"https:\/\/doi.org\/10.1177\/sage-journals-update-policy","source":"Crossref","is-referenced-by-count":15,"title":["Pediatric Hereditary Neuralgic Amyotrophy"],"prefix":"10.1177","volume":"3","author":[{"given":"Raymond","family":"Chuk","sequence":"first","affiliation":[{"name":"Discipline of Paediatrics, UnitingCare Health Clinical School, Wesley Hospital, Brisbane, Queensland, Australia"},{"name":"Department of Paediatrics, Wesley Hospital, Brisbane, Queensland, Australia"},{"name":"School of Medicine, University of Queensland, 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Pathogenesis"],"short-title":[],"issued":{"date-parts":[[2016,1,1]]},"references-count":17,"alternative-id":["10.1177\/2329048X16668970"],"URL":"https:\/\/doi.org\/10.1177\/2329048x16668970","relation":{},"ISSN":["2329-048X","2329-048X"],"issn-type":[{"value":"2329-048X","type":"print"},{"value":"2329-048X","type":"electronic"}],"subject":[],"published":{"date-parts":[[2016,1,1]]},"article-number":"2329048X16668970"}}