Comparative analysis between developmental and inflammatory odontogenic cysts: retrospective study and literature review
Purpose To assess epidemiological, clinical, and radiographic characteristics of
odontogenic cysts (OCs) in a South Brazilian sample and to compare the results with …
odontogenic cysts (OCs) in a South Brazilian sample and to compare the results with …
[HTML][HTML] Gorlin-Goltz syndrome–a medical condition requiring a multidisciplinary approach
M Kiwilsza, K Sporniak-Tutak - Medical science monitor …, 2012 - ncbi.nlm.nih.gov
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 …
inherited in a dominant autosomal way. The strongest characteristic of the disease includes …
Non-syndromic and syndromic keratocystic odontogenic tumors: systematic review and meta-analysis of recurrences
Abstract Background Keratocystic odontogenic tumors (KCOTs) are locally aggressive
benign tumors which occur in the bones of both jaws with a high recurrence rate. The aim of …
benign tumors which occur in the bones of both jaws with a high recurrence rate. The aim of …
Basal cell nevus syndrome or Gorlin syndrome
Basal cell nevus syndrome (BCNS) or Gorlin syndrome is a rare neurocutaneous syndrome
sometimes known as the fifth phacomatosis, inherited in autosomal dominant fashion with …
sometimes known as the fifth phacomatosis, inherited in autosomal dominant fashion with …
Benign jaw lesions
Benign lesions can develop from both odontogenic and nonodontogenic tissues in the
maxilla and mandible. Odontogenic lesions can arise from tooth-forming epithelium …
maxilla and mandible. Odontogenic lesions can arise from tooth-forming epithelium …
Gorlin-Goltz Syndrome: Case report and literature review
Gorlin-Goltz syndrome (GGS) is an infrequent multisystemic disease with an autosomal
dominant trait, with complete penetrance and variable expressivity, though sporadic cases …
dominant trait, with complete penetrance and variable expressivity, though sporadic cases …
Gorlin‐Goltz Syndrome
P Pandeshwar, K Jayanthi… - Case reports in dentistry, 2012 - Wiley Online Library
The Gorlin‐Goltz syndrome (GGS)(the nevoid basal cell carcinoma syndrome—NBCCS) is a
rare autosomal dominant syndrome caused due to mutations in the PTCH (patched) gene …
rare autosomal dominant syndrome caused due to mutations in the PTCH (patched) gene …
[HTML][HTML] An easily missed but life-threatening diagnosis: a case report of Gorlin syndrome
CS Kosmidis, C Michael, CM Mystakidou… - The American Journal …, 2023 - ncbi.nlm.nih.gov
Objective: Rare disease Background: Gorlin syndrome, also known as basal cell nevus
syndrome (BCNS), nevoid basal cell carcinoma syndrome (NBCCS), and Jaw cyst-Basal …
syndrome (BCNS), nevoid basal cell carcinoma syndrome (NBCCS), and Jaw cyst-Basal …
[HTML][HTML] Gorlin-Goltz syndrome: A case report and literature review
Gorlin-Goltz syndrome (GGS) is an infrequent multisystemic disease with an autosomal
dominant inherited disorder characterized by the presence of multiple keratocystic …
dominant inherited disorder characterized by the presence of multiple keratocystic …
[HTML][HTML] Gorlin–Goltz syndrome: A case series of 5 patients in North Indian population with comparative analysis of literature
Objective: In Indian scenario, Gorlin–Goltz syndrome (nevoid basal cell carcinoma
syndrome [NBCCS]) has been rarely reported. The clinical, radiological, and …
syndrome [NBCCS]) has been rarely reported. The clinical, radiological, and …