{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,4]],"date-time":"2026-09-04T11:12:06Z","timestamp":1788520326776,"version":"build-2803163510"},"reference-count":92,"publisher":"Wiley","issue":"3","license":[{"start":{"date-parts":[[2025,1,21]],"date-time":"2025-01-21T00:00:00Z","timestamp":1737417600000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by-nc-nd\/4.0\/"}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Clinical Exper Ophthalmology"],"published-print":{"date-parts":[[2025,4]]},"abstract":"<jats:title>ABSTRACT<\/jats:title>\n                  <jats:p>Hereditary vitreoretinopathies (HVRs), also known as hereditary vitreoretinal degenerations comprise a heterogeneous group of inherited disorders of the retina and vitreous, collectively and variably characterised by vitreal abnormalities, such as fibrillary condensations, liquefaction or membranes, as well as peripheral retinal abnormalities, vascular changes in some, an increased risk of retinal detachment and early\u2010onset cataract formation. The pathology often involves the vitreoretinal interface in some, while the major underlying abnormality is vascular in others. Recent advances in molecular diagnosis and identification of the responsible genes and have improved our understanding of the pathogenesis, risks and management of the HVRs. Clinically, HVRs can be classified according to the presence or absence of skeletal or other systemic abnormalities, retinal dysfunction or retinal vascular abnormalities [2]. There are some discrepancies in the literature regarding which diseases are included under the overarching term \u2018hereditary vitreoretinopathies\u2019. Conditions such as Stickler syndrome, Wagner syndrome and familial exudative vitreoretinopathy are generally included, while others such as autosomal dominant neovascular inflammatory vitreoretinopathy (ADNIV) and autosomal dominant vitreoretinochoroidapathy (ADVIRC) may not. In this review, we will discuss some historical aspects, the molecular pathogenesis, clinical features and management of diseases and syndromes commonly considered as HVRs.<\/jats:p>","DOI":"10.1111\/ceo.14494","type":"journal-article","created":{"date-parts":[[2025,1,21]],"date-time":"2025-01-21T21:25:23Z","timestamp":1737494723000},"page":"281-291","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":8,"title":["Hereditary Vitreoretinopathies: Molecular Diagnosis, Clinical Presentation and Management"],"prefix":"10.1111","volume":"53","author":[{"given":"Hashem H.","family":"Ghoraba","sequence":"first","affiliation":[{"name":"Cole Eye Institute Cleveland Clinic  Cleveland Ohio USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Jonathan","family":"Sears","sequence":"additional","affiliation":[{"name":"Cole Eye Institute Cleveland Clinic  Cleveland Ohio USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-8870-7673","authenticated-orcid":false,"given":"Elias I.","family":"Traboulsi","sequence":"additional","affiliation":[{"name":"Cole Eye Institute Cleveland Clinic  Cleveland Ohio USA"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"311","published-online":{"date-parts":[[2025,1,21]]},"reference":[{"key":"e_1_2_7_2_1","first-page":"1019","volume-title":"Retina","author":"Ding X.","year":"2023"},{"key":"e_1_2_7_3_1","first-page":"252","volume-title":"The Retina and Its Disorders","author":"Meredith S.","year":"2011"},{"key":"e_1_2_7_4_1","doi-asserted-by":"publisher","DOI":"10.1038\/eye.2008.38"},{"key":"e_1_2_7_5_1","first-page":"433","article-title":"Hereditary Progressive Arthro\u2010Ophthalmopathy","volume":"40","author":"Stickler G. 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