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The etio\u2010pathogenesis of PFE is due to the mutation of <jats:italic>PTH1R<\/jats:italic> gene. Clinical features such as infra\u2010occluded teeth, posterior open bite, lack of any cause or habit are usually attributed to diagnosing the condition, and a confirmatory diagnosis is done by the gene analysis of <jats:italic>PTH1R<\/jats:italic> gene. Treatment of such a condition is tricky as any application of orthodontic traction to teeth affected by PFE will not be successful and may cause ankylosis. This correspondence reviews and demonstrates the treatment of a case of PFE to restore function and esthetics to the best possible outcome.<\/jats:p>","DOI":"10.1002\/ccr3.5632","type":"journal-article","created":{"date-parts":[[2022,3,18]],"date-time":"2022-03-18T06:34:27Z","timestamp":1647585267000},"update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":9,"title":["Review and case report of the treatment in a young girl with primary failure of eruption"],"prefix":"10.1002","volume":"10","author":[{"given":"Mirna G.","family":"Awad","sequence":"first","affiliation":[{"name":"European University College DHCC Dubai UAE"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Lana","family":"Dalbah","sequence":"additional","affiliation":[{"name":"European University College DHCC Dubai 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