{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,27]],"date-time":"2026-08-27T14:17:28Z","timestamp":1787840248954,"version":"build-2784847793"},"reference-count":12,"publisher":"Ovid Technologies (Wolters Kluwer Health)","issue":"3","content-domain":{"domain":["lww.com","ovid.com"],"crossmark-restriction":true},"short-container-title":[],"published-print":{"date-parts":[[2022,5]]},"abstract":"<jats:sec>\n                    <jats:title\/>\n                    <jats:p>Familial cases of NMO are rare; and there are very few reports in association with Sjogren's syndrome. To report a familial case of NMO-Sjogren's Overlap syndrome. Mother and daughter presented with phenotypically different neurological episodes; mother had recurrent optic neuritis and myelitis with brainstem episode while the daughter had diencephalic presentation. Both were found to have AQP4 positivity with Ro-52 antibodies and positive Schirmer's test. They responded to steroids and plasma exchange. NMO associated with Sjogren's syndrome association suggests that apart from ethnicity both may have similar genetic predisposition and HLA-linkage.<\/jats:p>\n                  <\/jats:sec>","DOI":"10.4103\/0028-3886.349584","type":"journal-article","created":{"date-parts":[[2023,8,24]],"date-time":"2023-08-24T03:55:57Z","timestamp":1692849357000},"page":"1191-1193","update-policy":"https:\/\/doi.org\/10.1097\/lww.0000000000001000","source":"Crossref","is-referenced-by-count":2,"title":["Familial Neuromyelitis Optica and Sjogren's Overlap Syndrome-A Rare Case Report"],"prefix":"10.4103","volume":"70","author":[{"given":"VH","family":"Ganaraja","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"R","family":"Subasree","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"M","family":"Netravathi","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"276","reference":[{"key":"R1-58-20241013","doi-asserted-by":"crossref","first-page":"85","DOI":"10.1016\/j.msard.2019.01.032","article-title":"Clinical, neuroimaging and therapeutic response in AQP4-positive NMO patients from India","volume":"30","author":"Netravathi","year":"2019","journal-title":"Mult Scler Relat Disord"},{"key":"R2-58-20241013","doi-asserted-by":"crossref","first-page":"470","DOI":"10.4103\/0028-3886.103186","article-title":"Optic neuritis: Experience from a south Indian demyelinating disease 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Important insight","volume":"381","author":"Cheo","year":"2017","journal-title":"J Neurol Sci"},{"key":"R10-58-20241013","doi-asserted-by":"crossref","first-page":"171","DOI":"10.1111\/j.1399-0039.2008.01172.x","article-title":"Association of the HLA-DPB1 * 0501 allele with anti-aquaporin-4 antibody positivity in Japanese patients with idiopathic central nervous system demyelinating disorders","volume":"73","author":"Matsushita","year":"2009","journal-title":"Tissue Antigens"},{"key":"R11-58-20241013","doi-asserted-by":"crossref","first-page":"4","DOI":"10.2174\/1871524916666160229115047","article-title":"Neuromyelitis Optica (NMO IgG+) and Genetic Susceptibility, Potential Ethnic Influences","volume":"18","author":"Alonso","year":"2018","journal-title":"Cent Nerv Syst Agents Med Chem"},{"key":"R12-58-20241013","doi-asserted-by":"crossref","first-page":"1217","DOI":"10.1177\/1352458515574149","article-title":"Human leukocyte antigen association with neuromyelitis optica in a south 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