Gorlin-Goltz syndrome is a rare genetic condition showing a variable expressiveness. It is
inherited in a dominant autosomal way. The strongest characteristic of the disease includes …

Objective Nevoid basal cell carcinoma syndrome (NBCCS) is rarely reported in the Indian
population. We present the clinical and radiological features of 6 cases of NBCCS in Indian …

Gorlin-Goltz syndrome due to its high variability in expression are often not diagnosed as the
syndrome and often managed same as that of odontogenic keratocyst. But a more careful …

Gorlin-Goltz syndrome encompasses a variety of clinical signs and symptoms including
important oral manifestations which general dental practitioners should be aware of. In light …

Objective: In Indian scenario, Gorlin–Goltz syndrome (nevoid basal cell carcinoma
syndrome [NBCCS]) has been rarely reported. The clinical, radiological, and …

Gorlin–Goltz syndrome is an autosomal dominant inherited condition comprising the
principle triad of basal cell carcinomas, multiple jaw keratocysts, and skeletal anomalies …

Gorlin-Goltz syndrome or basal cell nevus syndrome is a comparatively rare syndrome
characterized by basal cell nevi, odontogenic keratocysts, and skeletal anomalies …

Background: Gorlin syndrome, also known as the basal cell nevus syndrome (OMIM#
109400), is a rare autosomal-dominant genetic disease. The disease, which shows mutation …

To date, there is no definite effective target therapy or cure for nevoid basal cell carcinoma
syndrome (NBCCS, Gorlin syndrome). Basal cell carcinoma is frequently the far most …

Gorlin-Goltz Syndrome is a genetic disorder characterized by a series of clinical changes,
including the presence of multiple odontogenic keratocysts and nevus basal cell …