Results 71 to 80 of about 1,019 (146)

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
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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

A Case Report of Gorlin-goltz Syndrome

Journal of Contemporary Medical Sciences, 2016
Nevoid basal cell carcinoma syndrome (Gorlin syndrome) is an autosomal dominant inherited condition that exhibits high penetrance and variable expressivity.
Shima Nafarzadeh, Fatemeh Mozaffari, Oveis Khakbaz   +2 more
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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
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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

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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Gorlin-Goltz Syndrome: case report and review of literature

Clinical and Biomedical Research, 2014
Description of a case report of Gorlin-Goltz Syndrome diagnosed in a male newborn who presented increased head circumference and bifid ribs. Mother and grandmother presented typical physical findings of the syndrome, including palmar pits, odontogenic ...
Adrianne Rahde Bischoff, Yina Mercedes Timana Delgado, Fabiano de Oliveira Poswar, Eduardo Tarasconi Ruschel, Eduardo Kohls Toralles, Gabriel Lona Curubeto Lona de Miranda, Mario Francisco Silveira Rita   +6 more
doaj   +2 more sources

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
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