{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,7,10]],"date-time":"2026-07-10T15:01:37Z","timestamp":1783695697425,"version":"3.55.0"},"reference-count":0,"publisher":"Knowledge E DMCC","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["CJN"],"abstract":"<jats:p>Background: Pathogenic variants in the RNASEH2B gene have been linked to Aicardi-Gouti\u00e8res syndrome type II (AGS-II), an early-onset encephalopathy that exhibits phenotypic overlaps with other neurodegenerative diseases, such as hereditary spastic paraplegia (HSP). A poor genotype-phenotype correlation, inconsistent findings in biomarker results of patients, and the challenge of distinguishing AGS-II from HSP underscore the necessity of performing comprehensive studies to address current difficulties in RNASEH2B-related cases. Here, through a detailed case report and comprehensive systematic review, we highlight clinical heterogeneity of RNASEH2B-related neurodegenerative cases and support the current view of considering RNASEH2B as an HSP-causing gene.\r\nMethods: Using whole exome sequencing (WES), we identified an RNASEH2B variant, c.529G&gt;A (p.Ala177Thr), in an Iranian patient suspected of having HSP, a mutation commonly reported in AGS-II. In contrast to AGS-II, clinical studies of the Iranian case were dominated by non-progressive HSP. A subsequent Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA)-guided review of RNASEH2B-related neurodegenerative disorders identified 49 relevant cases from 349 studies, revealing a variable spectrum of phenotypes. overlapping categories: \u201cRNASEH2B-related AGS\u201d, \u201catypical AGS-II\u201d, and \u201cRNASEH2B-related HSP\u201d. 95 cases were diagnosed as RNASEH2B-related AGS or atypical AGS-II; six were classified as RNASEH2B-related HSP. One case was asymptomatic, and another involved intrauterine fetal death.\r\nConclusion: The current study highlights the expanding phenotypic spectrum of RNASEH2B mutations, emphasizing their potential to manifest as isolated pure HSP (pHSP) rather than classical AGS. This study underscores the importance of raising clinical awareness and incorporating genetic testing, particularly for atypical RNASEH2B cases.<\/jats:p>","DOI":"10.18502\/cjn.v24i2.20683","type":"journal-article","created":{"date-parts":[[2026,1,5]],"date-time":"2026-01-05T10:28:56Z","timestamp":1767608936000},"source":"Crossref","is-referenced-by-count":1,"title":["Expanding the phenotypic spectrum  of RNASEH2B mutations: A new case  of pure hereditary spastic paraplegia  and a systematic review"],"prefix":"10.18502","author":[{"given":"Mohammad Reza","family":"Habibi-Kavashkohie","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Fardad","family":"Danaeefard","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Mohammad","family":"Rohani","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Afagh","family":"Alavi","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"7770","published-online":{"date-parts":[[2026,1,4]]},"container-title":["Current Journal of Neurology"],"original-title":[],"link":[{"URL":"https:\/\/publish.kne-publishing.com\/index.php\/CJN\/article\/download\/20683\/19394","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/publish.kne-publishing.com\/index.php\/CJN\/article\/download\/20683\/19394","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2026,2,25]],"date-time":"2026-02-25T10:48:22Z","timestamp":1772016502000},"score":1,"resource":{"primary":{"URL":"https:\/\/publish.kne-publishing.com\/index.php\/CJN\/article\/view\/20683"},"secondary":[{"URL":"https:\/\/cjn.tums.ac.ir\/article_40535.html","label":"UNIVERSITY"}]},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2026,1,4]]},"references-count":0,"URL":"https:\/\/doi.org\/10.18502\/cjn.v24i2.20683","relation":{},"ISSN":["2717-011X"],"issn-type":[{"value":"2717-011X","type":"electronic"}],"subject":[],"published":{"date-parts":[[2026,1,4]]}}}