{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,24]],"date-time":"2026-10-24T01:14:20Z","timestamp":1792804460218,"version":"4.5.0"},"reference-count":11,"publisher":"Ovid Technologies (Wolters Kluwer Health)","issue":"5","content-domain":{"domain":["lww.com","ovid.com"],"crossmark-restriction":true},"short-container-title":[],"published-print":{"date-parts":[[2023,9]]},"abstract":"<jats:p>\n                    Dystonia deafness syndrome (DDS) is a rare syndrome characterized by childhood onset sensorineural deafness followed by adult-onset dystonia. We here report the first case of DDS from India caused by\n                    <jats:italic toggle=\"yes\">ACTB<\/jats:italic>\n                    gene mutation presented with deafness, generalized dystonia and scoliosis who showed improvement after Deep brain stimulation.\n                  <\/jats:p>","DOI":"10.4103\/aian.aian_319_23","type":"journal-article","created":{"date-parts":[[2023,9,27]],"date-time":"2023-09-27T11:01:23Z","timestamp":1695812483000},"page":"766-768","update-policy":"https:\/\/doi.org\/10.1097\/lww.0000000000001000","source":"Crossref","is-referenced-by-count":8,"title":["Dystonia Deafness Syndrome: A Rare Deep Brain Stimulation Responsive Dystonia"],"prefix":"10.4103","volume":"26","author":[{"given":"Sruthi","family":"Kola","sequence":"first","affiliation":[{"name":"Department of Parkinson\u2019s Disease and Movement Disorders Research Centre (PDMDRC), Citi Neuro Centre, Telangana, India"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Rukmini Mridula","family":"Kandadai","sequence":"additional","affiliation":[{"name":"Department of Parkinson\u2019s Disease and Movement Disorders Research Centre (PDMDRC), Citi Neuro Centre, Telangana, India"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Mansi","family":"Kashyap","sequence":"additional","affiliation":[{"name":"Department of Parkinson\u2019s Disease and Movement Disorders Research Centre (PDMDRC), Citi Neuro Centre, Telangana, India"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Sai","family":"Deepak","sequence":"additional","affiliation":[{"name":"Department of Parkinson\u2019s Disease and Movement Disorders Research Centre (PDMDRC), Citi Neuro Centre, Telangana, India"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"VVSRK","family":"Prasad","sequence":"additional","affiliation":[{"name":"Department of Parkinson\u2019s Disease and Movement 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variant in ACTB, p.Arg183Trp, causes juvenile-onset dystonia, hearing loss, and developmental delay without midline malformation","volume":"2017","author":"Conboy","year":"2017","journal-title":"Case Rep Genet"},{"key":"R10-20260512","doi-asserted-by":"crossref","first-page":"195","DOI":"10.1007\/s10048-017-0521-9","article-title":"Molecular diversity of combined and complex dystonia: Insights from diagnostic exome sequencing","volume":"18","author":"Zech","year":"2017","journal-title":"Neurogenetics"},{"key":"R11-20260512","doi-asserted-by":"crossref","first-page":"86","DOI":"10.1002\/mdc3.12854","article-title":"Expanding the phenotype of dystonia-deafness syndrome caused by ACTB gene mutation","volume":"7","author":"Freitas","year":"2019","journal-title":"Mov Disord Clin Pract"},{"key":"R12-20260512","doi-asserted-by":"crossref","first-page":"122","DOI":"10.1002\/mdc3.13358","article-title":"Dystonia-deafness syndrome: ACTB pathogenic variant in an argentinean 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