{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,16]],"date-time":"2026-09-16T07:04:17Z","timestamp":1789542257650,"version":"build-2803163510"},"reference-count":49,"publisher":"Wiley","issue":"1","license":[{"start":{"date-parts":[[2026,9,15]],"date-time":"2026-09-15T00:00:00Z","timestamp":1789430400000},"content-version":"vor","delay-in-days":257,"URL":"https:\/\/creativecommons.org\/licenses\/by\/4.0\/"},{"start":{"date-parts":[[2026,1,1]],"date-time":"2026-01-01T00:00:00Z","timestamp":1767225600000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/doi.wiley.com\/10.1002\/tdm_license_1.1"}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Case Reports in Dentistry"],"published-print":{"date-parts":[[2026,1]]},"abstract":"<jats:sec>\n                    <jats:title>Introduction<\/jats:title>\n                    <jats:p>Freeman\u2013Burian syndrome (FBS) is a congenital myopathic craniofacial condition that often includes features outside the craniofacial region. Among the craniofacial manifestations of FBS, the severely reduced oral aperture stands out as one of the most functionally limiting features of the condition. This marked constriction compromises nutritional intake, speech clarity, oral health maintenance, and airway access. Additionally, the distinctive \u201cpursed\u2010lip\/whistling\u201d facial appearance imposes considerable psychological and social challenges.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Case Presentation<\/jats:title>\n                    <jats:p>An 11\u2010year\u2010old girl was evaluated for challenges consuming solid food and prolonged meal duration, issues that had persisted since early childhood. Physical assessment demonstrated characteristic FBS findings meeting the diagnostic criteria, including microstomia (interlabial distance of 24\u2009mm at maximum opening), an H\u2010shaped chin defect, hypoplastic nasal alae, and prominent nasolabial creases. Additional findings included mild thoracic scoliosis and reduced stature.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Management<\/jats:title>\n                    <jats:p>The patient underwent bilateral surgical widening of the oral commissures employing Converse\u2032s V\u2010Y mucosal advancement flap technique to enlarge the restricted mouth opening. Fiber\u2010optic assisted nasal intubation was utilized for airway management.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusion<\/jats:title>\n                    <jats:p>Optimal outcomes depend on an accurate and early diagnosis and understanding of the myopathic craniofacial basis and origin of the syndrome, together with an anticipatory and coordinated team\u2010based strategy. Management must specifically target the fibrous constricting bands, ensure an adequate oral aperture for nutrition and dental care, support long\u2010term needs of the patient, and incorporate careful preparation for anesthesia\u2010associated complications.<\/jats:p>\n                  <\/jats:sec>","DOI":"10.1155\/crid\/2707697","type":"journal-article","created":{"date-parts":[[2026,9,16]],"date-time":"2026-09-16T06:29:19Z","timestamp":1789540159000},"update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":0,"title":["Microstomia Correction in an 11\u2010Year\u2010Old Girl With Freeman\u2013Burian 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