TY - JOUR AU - Hashmi, Atif Ali AU - Edhi, Muhammad Muzzammil AU - Faridi, Naveen AU - Hosein, Mervyn AU - Khan, Mehmood PY - 2016 DA - 2016/07/22 TI - Mutiple keratocystic odontogenic tumors (KCOT) in a patient with Gorlin syndrome: a case report with late presentation and absence of skin manifestations JO - BMC Research Notes SP - 357 VL - 9 IS - 1 AB - Gorlin syndrome is a rare autosomal dominant syndrome characterized by multiple basal cell carcinomas, keratocystic odontogenic tumors (KOT) and falx cerebral calcifications, which occur due to mutation in PTCH gene. SN - 1756-0500 UR - https://doi.org/10.1186/s13104-016-2166-4 DO - 10.1186/s13104-016-2166-4 ID - Hashmi2016 ER -