{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,11,15]],"date-time":"2025-11-15T00:25:17Z","timestamp":1763166317853,"version":"3.45.0"},"reference-count":21,"publisher":"Georg Thieme Verlag KG","issue":"01","license":[{"start":{"date-parts":[[2025,1,20]],"date-time":"2025-01-20T00:00:00Z","timestamp":1737331200000},"content-version":"vor","delay-in-days":19,"URL":"https:\/\/creativecommons.org\/licenses\/by-nc-nd\/4.0\/"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["J Neurol Surg Rep"],"published-print":{"date-parts":[[2025,1]]},"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:p>Background\u2003A rare variant of congenital aqueductal stenosis (CAS) is known as adult-onset CAS, characterized by the emergence of symptoms during adulthood.<\/jats:p>\n                  <jats:p>Case Description\u2003A 35-year-old man presented complaining of acute-onset headache and vomiting. Magnetic resonance imaging of the brain revealed an acute hydrocephalus due to an aqueductal web. The patient was treated with a ventriculoperitoneal shunt and doing well. His condition was complicated by subdural hematoma as a result of overshunting, which was treated by frontoparietal craniotomy and eventually, he underwent valve revision to a programmable valve.<\/jats:p>\n                  <jats:p>Conclusion\u2003Additional research is needed to gain a deeper understanding of the hypothesis related to adult aqueductal stenosis. This will help shed light on the asymptomatic childhood phase and potentially reduce complications by identifying late CAS early.<\/jats:p>","DOI":"10.1055\/s-0044-1788037","type":"journal-article","created":{"date-parts":[[2025,1,20]],"date-time":"2025-01-20T19:53:29Z","timestamp":1737402809000},"page":"e4-e7","source":"Crossref","is-referenced-by-count":0,"title":["Late Presentation of Congenital Aqueduct Stenosis in Adulthood with High-Riding Basilar Artery: Case Report"],"prefix":"10.1055","volume":"86","author":[{"ORCID":"https:\/\/orcid.org\/0009-0002-2885-5521","authenticated-orcid":false,"given":"Hassan Mohammed","family":"Alturiki","sequence":"additional","affiliation":[{"name":"Faculty of Medicine, King Faisal University, Al-Ahsa, Saudi Arabia"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Batool M.","family":"Alqudaihi","sequence":"additional","affiliation":[{"name":"Faculty of Medicine, Hacettepe University, Ankara, Turkey"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Shima","family":"Alboesa","sequence":"additional","affiliation":[{"name":"Faculty of Medicine, King Faisal University, Al-Ahsa, Saudi Arabia"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Abdullah H.","family":"Alramadan","sequence":"additional","affiliation":[{"name":"Department of Neurosurgery and Spine Surgery, Qatif Central Hospital, Qatif, Saudi Arabia"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"194","published-online":{"date-parts":[[2025,1,20]]},"reference":[{"key":"ref1","first-page":"933","volume-title":"Aqueductal stenosis and hydrocephalus","author":"P Spennato","year":"2018"},{"issue":"04","key":"ref2","doi-asserted-by":"crossref","first-page":"617","DOI":"10.1007\/s00381-016-3029-y","article-title":"Hydrocephalus in aqueductal stenosis\u2013a retrospective outcome analysis and proposal of subtype classification","volume":"32","author":"I Rodis","year":"2016","journal-title":"Childs Nerv Syst"},{"issue":"09","key":"ref3","doi-asserted-by":"crossref","first-page":"176","DOI":"10.36349\/easjmb.2022.v05i09.001","article-title":"Genetics of hydrocephalus (HC)","volume":"5","author":"I Naureen","year":"2022","journal-title":"East African Scholars Multidisciplinary Bulletin"},{"issue":"01","key":"ref4","doi-asserted-by":"crossref","first-page":"101","DOI":"10.1016\/S0022-510X(98)00097-5","article-title":"Familial congenital hydrocephalus and aqueduct stenosis with probably autosomal dominant inheritance and variable expression","volume":"158","author":"W I Verhagen","year":"1998","journal-title":"J Neurol Sci"},{"issue":"12","key":"ref5","doi-asserted-by":"crossref","first-page":"1322","DOI":"10.1136\/jnnp.37.12.1322","article-title":"Benign aqueduct stenosis in adults","volume":"37","author":"M JG Harrison","year":"1974","journal-title":"J Neurol Neurosurg Psychiatry"},{"issue":"02","key":"ref6","doi-asserted-by":"crossref","first-page":"181","DOI":"10.1016\/j.mjafi.2012.02.002","article-title":"A rare case of congenital aqueductal stenosis","volume":"69","author":"K S Brar","year":"2013","journal-title":"Med J Armed Forces India"},{"issue":"05","key":"ref7","doi-asserted-by":"crossref","first-page":"546","DOI":"10.3171\/jns.1975.43.5.0546","article-title":"Clinical manifestations of aqueductal stenosis in adults","volume":"43","author":"J R Little","year":"1975","journal-title":"J Neurosurg"},{"issue":"03","key":"ref8","doi-asserted-by":"crossref","first-page":"145","DOI":"10.1111\/j.1600-0404.2005.00379.x","article-title":"How should primary aqueductal stenosis in adults be treated? 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