Abstract
Gorlin–Goltz syndrome, is an uncommon genetic condition characterized by the presence
of multiple odontogenic keratocysts of jaws along with several other abnormal, cutaneous,
ophthalmic, and osseous displays. This syndrome is also acknowledged by various names,
such as nevoid basal cell carcinoma syndrome, jaw cyst, and bifid rib syndrome. This
article illustrates about the clinical, radiological, and histological diagnostic
findings and the multidisciplinary approach of treatment given to one such rare case
of Gorlin–Goltz syndrome.
Keywords
Gorlin–Goltz syndrome - multiple odontogenic keratocyst syndrome - nevoid basal cell
carcinoma syndrome - Gorlin’s syndrome
