{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,2,23]],"date-time":"2026-02-23T14:22:12Z","timestamp":1771856532805,"version":"3.50.1"},"reference-count":27,"publisher":"Frontiers Media SA","license":[{"start":{"date-parts":[[2026,2,23]],"date-time":"2026-02-23T00:00:00Z","timestamp":1771804800000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"content-domain":{"domain":["frontiersin.org"],"crossmark-restriction":true},"short-container-title":["Front. Med."],"abstract":"<jats:p>This study presents a case of restrictive strabismus with ipsilateral enophthalmos secondary to a supernumerary extraocular muscle (SEOM). Orbital MRI and posterior segment OCT provided direct imaging evidence that delineated the posterior origin of the SEOM and its mechanical traction on the globe, while also revealing concomitant hypoplasia of the medial and lateral rectus muscles. These findings together elucidate the mechanical basis of both ocular motility restriction and enophthalmos in this case. Genetic analysis revealed a pathogenic duplication in the 22q11.21 region, which\u2014to our knowledge\u2014is the first reported association linking this variant to SEOM-related restrictive strabismus, thereby expanding the ocular phenotypic spectrum of the 22q11.2 duplication syndrome. The discussion underscores that surgical intervention carries substantial risk due to the deep, optic-nerve-adjacent location of the SEOM and the presence of rectus muscle hypoplasia, compounded by the reportedly poorer prognosis associated with posterior SEOM (Type 3). Hence, conservative management was advised. This case highlights the central diagnostic role of MRI and offers novel insights into the etiology and individualized management of anomalous orbital structures.<\/jats:p>","DOI":"10.3389\/fmed.2026.1782101","type":"journal-article","created":{"date-parts":[[2026,2,23]],"date-time":"2026-02-23T13:36:27Z","timestamp":1771853787000},"update-policy":"https:\/\/doi.org\/10.3389\/crossmark-policy","source":"Crossref","is-referenced-by-count":0,"title":["Case Report: From imaging to genetics: a case of congenital restrictive strabismus with SEOM expands the 22q11.2 duplication syndrome phenotype"],"prefix":"10.3389","volume":"13","author":[{"given":"Xingyuan","family":"Wei","sequence":"first","affiliation":[{"name":"Xiamen Eye Center and Eye Institute of Xiamen University, School of Medicine","place":["Xiamen, China"]}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Ruxin","family":"Gao","sequence":"additional","affiliation":[{"name":"Xiamen Eye Center and Eye Institute of 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