Peri-apical Sinus, A Leading Edge of Gorlin–Goltz Syndrome: Case Report
V. D. Tripathi, A. K. Nagarajappa, V. S. Chauhan, K. T. Chandrashekar, R. Mishra & S. K. Tripathi · Journal of Advances in Medicine and Medical Research · 2017
Gorlin–Goltz syndrome is an autosomal dominant disorder, with mutations in the patched tumor suppressor gene (PTCH1) leading to a wide range of developmental anomalies and neoplasms of cutaneous, dental, osseous, ophthalmic and neurological origin. It commonly presents as multipl...
Open access
Research Article
10.9734/BJMMR/2017/32469