{Reference Type}: Case Reports
{Title}: Isolated Congenital Camptodactyly and Temporomandibular Joint Articular Disc Displacement.
{Author}: Aponte CA;Hoffman A;Moussa S;Norvell N;Khoury ZH;
{Journal}: Cureus
{Volume}: 14
{Issue}: 11
{Year}: Nov 2022
暂无{DOI}: 10.7759/cureus.31658
{Abstract}: The development of craniofacial structures is complex and involves multiple cellular and molecular interactions. We report a case of congenital camptodactyly in a female who subsequently developed chronic tinnitus and temporomandibular joint dysfunction. This report describes the clinicoradiographic features and surgical management of the facial skeletal manifestations, along with postoperative rehabilitation. Furthermore, a concise review of similar literature raises the question of whether this complex of manifestations represents a new entity or a minimal manifestation of a previously characterized syndrome. As such, a possible developmental association between camptodactyly and temporomandibular joint dysfunction is suggested.