Results 81 to 90 of about 1,227,204 (147)

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

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

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
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