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Journal of Indian Academy of Oral Medicine and Radiology, 2010 Gorlin-Goltz syndrome, also known as basal cell nevus syndrome, is an uncommon autosomal dominant inherited disorder characterized by numerous basal cell carcinomas, odontogenic keratocysts, and musculoskeletal malformation. It is occasionally associated
M K Sunil +3 more
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Odontogenic keratocysts are an important clue for diagnosing basal cell nevus syndrome. [PDF]
Nagoya J Med Sci, 2021 Basal cell nevus syndrome (BCNS) is an autosomal dominant skin disorder characterized by multiple basal cell nevi. Patients with BCNS tend to develop basal cell carcinoma (BCC) and frequently show skeletal abnormalities.
Kaibuchi-Ando K +8 more
europepmc +2 more sources
Basal cell carcinoma and basal cell nevus syndrome:optimizing treatment and care [PDF]
, 2023 This study aims to optimize the treatment of basal cell carcinoma and basal cell nevus syndrome. Studies show that surgical excision is more effective than imiquimod 5% cream.
Verkouteren, Babette Jacoba Anna
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BASAL CELL NEVUS SYNDROME [PDF]
American Journal of Roentgenology, 1968 The manifestations of an inherited syndrome with emphasis on the roentgenographic findings have been described. Thirteen additional cases are reported and an example of extensive involvement of one family is presented. The importance of recognition of this syndrome, especially in children, because of the malignant potential and the need for genetic ...
C J, Rater, A C, Selke, E F, Van Epps
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18F-FDG PET/CT and Whole-Body Bone Scan Findings in Gorlin–Goltz Syndrome
Diagnostics, 2023 Gorlin–Goltz syndrome (basal cell nevus syndromes) is an uncommon, autosomal dominant inherited disorder characterized by developing basal cell carcinomas from a young age.
Miju Cheon, Jang Yoo, Kyu-Bok Kang
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Syndrome in question: Gorlin-Goltz syndrome [PDF]
Anais Brasileiros de Dermatologia, 2016 : The Nevoid Basal Cell Carcinoma Syndrome (NBCCS) is an uncommon disorder caused by a mutation in Patched, tumor suppressor gene. It is mainly characterized by numerous early onset basal cell carcinomas, odontogenic cysts of jaw and skeletal ...
Pauline Lyrio Ribeiro +4 more
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Phenotypic spectrum of a patient with Gorlin’s syndrome and role of dermoscopy in the early detection of basal cell carcinomas [PDF]
Anais Brasileiros de Dermatologia, 2015 Gorlin's syndrome is an autosomal dominant disorder, mainly characterized by the presence of multiple and early-onset basal cell carcinomas, odontogenic keratocysts and palmoplantar pits.
Catarina Moreira +4 more
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Axillary basal cell carcinoma in patients with Goltz-Gorlin syndrome: report of basal cell carcinoma in both axilla of a woman with basal cell nevus syndrome and literature review [PDF]
, 2014 Background: Basal cell carcinoma of the axilla, an area that is not usually exposed to the sun, is rare. Individuals with basal cell nevus syndrome, a disorder associated with a mutation in the patch 1 (PTCH1) gene, develop numerous basal cell carcinomas.
Cohen, Philip R, +2 more
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Gorlin-Goltz syndrome in an older black adult. Case Report
Revista de la Facultad de Medicina, 2021 Introduction: Gorlin-Goltz syndrome (GGS), or basal cell nevus syndrome (BCNS), is a rare genetic disease that induces the development of odontogenic keratocysts, skeletal malformations and neoplasms, especially multiple and recurrent basal cell ...
Mauricio Andrés Uribe-Valencia +3 more
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