 The study examined 33 patients diagnosed with binder syndrome at the Royal Children's Hospital of Melbourne and found that they had nasomaxillary hypoplasia, characterized by reduced antroposterior lengths of the anterior cranial base and maxilla, and a majority of them had a class 3 skeletal relationship. Despite this, their orthodontic and surgical treatment is typically carried out within specialized units. This article was authored by Carrick Barbra, Woods Michael, and Scott Peter.