Results 91 to 100 of about 1,227,204 (153)

Headache as the presenting manifestation of Gorlin-Goltz syndrome with diastematomyelia: A case report. [PDF]

Neurol Clin Neurosci, 2023
Ghosh R, León-Ruiz M, Purkait S, Roy D, Ghosh T, Benito-León J.   +5 more
europepmc   +1 more source

An uncommon disorder with multiple skeletal anomalies: Gorlin-Goltz syndrome

The Turkish Journal of Pediatrics, 2014
Gorlin-Goltz syndrome is an uncommon disorder transmitted through autosomal dominant inheritance. This syndrome is characterized by multiple odontogenic keratocysts, along with congenital skeletal anomalies and basal cell carcinomas. A 16-year-old
Onur Keçeli, İlke Coskun-Benlidayı, M Emre Benlidayı, Özgür Erdoğan   +3 more
doaj  

Gorlin-Goltz syndrome associated with bilateral cleft lip and palate

Revista Cubana de Estomatología, 2015
Introduction: Gorlin Goltz Syndrome (GGS) is an autosomal dominant inherited disorder. One of the minor criteria for such syndrome is the cleft lip and palate (CL/CP).
Noemí Lorena Leiva Villagra, Sebastián Alejandro Véliz Méndez, Leonardo Esteban González Escobar, Carolina Andrea Salazar Ponce   +3 more
doaj  

Gorlin Goltz Syndrome: Beware of Melanoma. [PDF]

Dermatol Pract Concept, 2022
Russo F, Liso FG, Santi F, Provvidenziale L, Taddeucci P, Rubegni P.   +5 more
europepmc   +1 more source

Oral and Maxillofacial Surgeon's Perspective on Gorlin-Goltz Syndrome - A Report of Two Cases. [PDF]

Ann Maxillofac Surg, 2022
Wadde KR, Ghodke MN, Chowdhar AS, Nadkarni SP, Venkatakrishnan L, Sarda A.   +5 more
europepmc   +1 more source

Gorlin-Goltz syndrome without cutaneous manifestations. [PDF]

Pan Afr Med J, 2021
Singh RK, Mishra GV.
europepmc   +1 more source

Multidisciplinary approach to Gorlin-Goltz syndrome: from diagnosis to surgical treatment of jawbones. [PDF]

Maxillofac Plast Reconstr Surg, 2022
Spadari F, Pulicari F, Pellegrini M, Scribante A, Garagiola U.   +4 more
europepmc   +1 more source

Manifestations of Gorlin-Goltz syndrome

, 2014
INTRODUCTION: Gorlin-Goltz syndrome is an uncommon hereditary condition caused by mutations in the PTCH1 gene causing a wide range of developmental abnormalities. Multiple basal cell carcinomas, palmoplantar pits and jaw cysts are cardinal features. Many
Larsen, Anne Kristine, Hertz, Jens Michael, Mikkelsen, Dorthe, Bygum, Anette; id_orcid   +3 more
core   +1 more source

A Vigilant Diagnostic Approach to Gorlin Goltz Syndrome: Case Report

Background: Gorlin-Goltz Syndrome (GGS), or Nevoid Basal Cell Carcinoma Syndrome, is a rare autosomal dominant disorder characterized by odontogenic keratocysts, skeletal abnormalities, and intracranial calcifications.
Anmol Kaur Ghuman, Ananya Rusia, Subhasish Subhasish, Amandeep Singh Gill, Priyanko Chakraborty, Saptasikha Das, Kanwarjot Singh Kohli, Gursimrat Kaur, Sandeep Ghosh, Surbhi Malik, Nishant Shahi, Monali Sah   +11 more
core   +1 more source

Immunoexpression of CXCL12 and CXCR4 in sporadic and Gorlin-Goltz syndrome-related odontogenic keratocysts. [PDF]

J Clin Exp Dent, 2022
de Lima WP, Andrade AO, Cavalcante RB, Nogueira RL, Alves PM, Nonaka CF, Gordón-Núñez MA.   +6 more
europepmc   +1 more source