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Ocular manifestations in Gorlin-Goltz syndrome. [PDF]
Orphanet J Rare Dis, 2019 Moramarco A +8 more
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Novel PTCH1 Gene Mutation in a Patient with Gorlin-Goltz Syndrome. [PDF]
Ann Dermatol, 2019 Ozlu E +8 more
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Gorlin-Goltz Syndrome: A Case Report and Literature Review. [PDF]
Cureus, 2019 Al-Jarboua MN +3 more
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A Unique Case of Gorlin-Goltz Syndrome with Associated Sotos Syndrome.
Ann Maxillofac Surg, 2020 Lata J, Kaur J.
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Multidisciplinary oral rehabilitation of an adolescent suffering from juvenile Gorlin-Goltz syndrome - a case report. [PDF]
Head Face Med, 2019 Nilius M +4 more
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An enigma of Gorlin-Goltz syndrome: Two cases reported in mother and daughter.
J Oral Maxillofac Pathol, 2019 Sahu S, Sahoo S, Banerjee R, Ghosh S.
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Gorlin-Goltz Syndrome: A Rare Case Report.
Contemp Clin Dent, 2018 Kumar NN +3 more
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Journal of Datta Meghe Institute of Medical Sciences University, 2022
Gorlin-Goltz syndrome (GGS) is a rare autosomal dominant condition. Diverse incidence rates of this syndrome have been reported all over the world. It is estimated to occur 1 in 50,000–150,000. GGS is of particular interest to dental surgeons and maxillofacial radiologists because of their association with odontogenic keratocysts (OKC).
Pragati Anupkumar Bhargava +2 more
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Gorlin-Goltz syndrome (GGS) is a rare autosomal dominant condition. Diverse incidence rates of this syndrome have been reported all over the world. It is estimated to occur 1 in 50,000–150,000. GGS is of particular interest to dental surgeons and maxillofacial radiologists because of their association with odontogenic keratocysts (OKC).
Pragati Anupkumar Bhargava +2 more
openaire +1 more source
Acta dermatovenerologica Alpina, Pannonica, et Adriatica, 2007
Gorlin-Goltz syndrome, also known as basal cell nevus syndrome, is an uncommon, autosomal dominant inherited disorder, which is characterized by numerous basal cell carcinomas, maxillary keratocysts, and musculoskeletal malformations. Occasionally, it is associated with aggressive basal cell carcinomas and internal malignancies.
Binić, Ivana +4 more
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Gorlin-Goltz syndrome, also known as basal cell nevus syndrome, is an uncommon, autosomal dominant inherited disorder, which is characterized by numerous basal cell carcinomas, maxillary keratocysts, and musculoskeletal malformations. Occasionally, it is associated with aggressive basal cell carcinomas and internal malignancies.
Binić, Ivana +4 more
openaire +4 more sources
Dermoscopy in Gorlin-Goltz Syndrome
Dermatologic Surgery, 2006Gorlin-Goltz syndrome (GGS) is an autosomal dominant disorder mainly characterized by the presence of multiple basal cell carcinomas (BCC), odontogenic keratocysts of the jaw, and volar pits. This syndrome is associated with a wide spectrum of developmental anomalies and neoplasms.To describe dermoscopic characteristics of cutaneous GGS lesions ...
I, Kolm, S, Puig, P, Iranzo, J, Malvehy
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