\papertypeOriginal ArticleCongenital nasal (septal) polyp in a term neonate: a case report and review of the literatureSurasak Puvabanditsin, MDAssociate Professor of PediatricsDepartment of PediatricsRutgers Robert Wood Johnson Medical SchoolNew Brunswick, New JerseyAli G Saad, MD ags210@rwjms.rutgers.eduDepartment of PathologyRutgers Robert Wood Johnson Medical SchoolNew Brunswick, New JerseyArun Sangam, MBA arun.sangam@hmhn.orgDepartment of PediatricsHackensack Meridian School of MedicineNutley, New JerseyAnthony Poltronetti, MD ap2536@rutgers.eduDepartment of PediatricsRutgers Robert Wood Johnson Medical SchoolNew Brunswick, New JerseySu Young Park, MD sp2521@rwjms.rutgers.eduDepartment of PediatricsRutgers Robert Wood Johnson Medical SchoolNew Brunswick, New JerseyAmrryn Halari, M.B.B.S ah1452@rwjms.rutgers.eduDepartment of PediatricsRutgers Robert Wood Johnson Medical SchoolNew Brunswick, New JerseyRajeev Mehta, MD mehtara@rwjms.rutgers.eduDepartment of PediatricsRutgers Robert Wood Johnson Medical SchoolNew Brunswick, New JerseyCorrespondence about the manuscript or reprint:Surasak Puvabanditsin, MDRutgers Robert Wood Johnson Medical School,1 Robert Wood Johnson Place, MEB 396New Brunswick, NJ 08901Tel. (732) 235-5691, FAX (732) 235-5688

We report a preterm male neonate presenting with a skeletal dysplasia associated with multiple congenital anomalies. Radiologic findings and genetic studies are consistent with spondylocostal dysostosis (SCD) and autosomal dominant brachydactyly. This is the first case report of spondylocostal dysostosis and brachydactyly associated with TBX6 and IHH variants.