Abstract
Gorlin–Goltz syndrome is an infrequent multisystemic disease that is inherited in an autosomal dominant way showing a high level of penetrance & variable expressiveness. It is about a multisystemic process that is characterized by the presence of odontogenic keratocysts in the jaws, multiple basal cell nevi or carcinomas, palmar and/or plantar pits & calcification of falx cerebri. Diagnosis of Gorlin–Goltz syndrome is made by having two major criteria or one major & two minor criteria. Here, we report a case of a 11-year-old girl suffering from this syndrome presenting with two new entities namely bifid tongue & partial ankyloglossia.
Full Text 
Sign-in/Register to access full text options
Sign-in/Register to access full text options 
Published version (
Free)
Free) 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a call
