Results 81 to 90 of about 1,227,185 (144)

Gorlin-goltz syndrome, an incidental finding: A rare case report

Journal of Indian Academy of Oral Medicine and Radiology, 2012
Gorlin-Goltz syndrome is an uncommonly found rare disease which shows various possible diverse manifestations of multisystem anomalies, high degree penetration rate with variable expressiveness at least on three body systems.
Sanyasi Gandhiraj
doaj  

Anaesthetic management in Gorlin-Goltz syndrome

, 2012
Gorlin-Goltz syndrome is a rare autosomal-dominant syndrome related to mutation in " Patched" tumour suppressor gene on chromosome 9. Basocellular carcinomas, odontogenic keratocysts, palmar and/or plantar pits and ectopic calcifications of the falx ...
Kundan S Gosavi, Surbhi D Mundada
core   +1 more source

Medulloblastoma with Extensive Nodularity in a Child with Gorlin Syndrome - Case Report from Regional Cancer Centre

Clinical Pediatric Hematology-Oncology
Gorlin syndrome, also known as Gorlin-Goltz syndrome, nevoid basal cell carcinoma syndrome (NBCCS), or basal cell nevus syndrome, is a rare autosomal dominant cancer predisposition disorder characterized by high penetrance and variable expressivity.
M. Vijay Krishnan, Appaji Lingegowda, Arun Kumar, Prakruthi S. Kaushik, Meena Haldorai, R. Nikila, Avinash Thummalapalli, T. M. Surekha   +7 more
doaj   +1 more source

GORLİN-GOLTZ SENDROMU

, 2023
Giriş-Amaç: Bazal hücreli karsinom sendromu olarak da bilinen Gorlin-Goltz sendromu otozomal dominant (OD) geçiş gösteren, nadir görülen multisistemik hastalıktır (1).
Çelik, Zafer, Atlanoğlu, Şahinde, Çakmak, Zeynep, Tutuğ Güven, Hazan   +3 more
core  

Gorlin Goltz Syndrome : A Review

Journal of Indian Academy of Oral Medicine and Radiology, 2003
Gorlin syndrome is a rare autosomal dominant disorder characterized by multiple basal cell carcinomas, odontogenic keratocysts, tumors, and systemic anomalies.
M S Deepa, C Raphy Paul, Anita Balan
doaj  

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  

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

Management of pedal fibrovascular papillomas in Goltz-Gorlin syndrome. [PDF]

JAAD Case Rep, 2016
DeCrescenzo AJ, Bachilo OS, Cole EL, Wilkerson MG.   +3 more
europepmc   +1 more source