Results 91 to 100 of about 1,227,254 (171)

Gorlin-Goltz Syndrome: Report of a Rare Case with an Update on the Review of the Literature. [PDF]

Contemp Clin Dent, 2023
Attur S, Patel JK, Attur K, Menat S.
europepmc   +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

Gorlin-Goltz Syndrome - A Concatenation of Six Case Reports. [PDF]

Ann Maxillofac Surg, 2023
Marimallappa TR, Rao K, Kumar KA, Kumar RM, Pal S, Jha M.   +5 more
europepmc   +1 more source

Siblings with Gorlin-Goltz syndrome associated with cardiac tumors: a case report and review of literature. [PDF]

Orphanet J Rare Dis, 2023
Wilke PI, Biermann D, Grafmann M, Kozlik-Feldmann R, Papingi D, Sachweh JS, Stute F, Olfe J.   +7 more
europepmc   +1 more source

Gorlin-Goltz Syndrome [PDF]

Türk Pediatri Arşivi, 2016
Betul Sereflican, Bengu Tuman, Murat Sereflican, Siddika Halicioglu, Gulzade Ozyalvacli, Seval Bayrak, Sevil Bilir Goksugur, Nadir Goksugur   +7 more
openaire   +2 more sources

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  

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