Treacher Collins Syndrome: Diagnosis and Management of a Case

Treacher Collins syndrome (TCS) is a genetic disorder resulting in a congenital craniofacial malformation. Patients typically present with oblique palpebral fissures, inferior palpebral colobomas, microtia, and malar and mandibular hypoplasia. This autosomal dominant disorder has variable phenotypic expression, and patients do not exhibit associated developmental delays or neurological disease. Management of these patients requires a multidisciplinary team from birth to adulthood. Appropriate planning, support, and surgical techniques are essential to optimize patient outcomes. We report a case of TCS treated in the maxillo-facial surgery departement of the university hospital of Ibn Sina of Rabat.