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Oral and Maxillofacial Surgery Cases, 2022 Objective: This case series reports the clinical presentation and management of multiple odontogenic keratocysts (OKCs) in patients with Gorlin Goltz syndrome and in non-syndromic patients.
Omer Sefvan Janjua +4 more
doaj +1 more source
Familial multiple basal cell carcinoma (Gorlin′s syndrome): A case report of a father and son
Indian Journal of Dermatology, 2013 Gorlin syndrome is a rare familial disorder characterized by numerous basal cell carcinomas along with facial and skeletal findings. Here, we report a father and son case, presented with features of Gorlin syndrome.
Balkrishna Nikam +3 more
doaj +1 more source
Gorlin–Goltz Syndrome: A Case Report and Literature Review with PTCH1 Gene Sequencing
Archives of Plastic Surgery, 2023 Gorlin–Goltz syndrome, also known as nevoid basal cell carcinoma syndrome, is an autosomal dominant disease characterized by multisystemic developmental defects caused by pathogenic variants such as patched-1 (PTCH1) gene variants and/or SUFU gene ...
Hyo Seong Kim +4 more
doaj +1 more source
Annals of Medical and Health Sciences Research, 2014 The Gorlin-Goltz syndrome (GGS) (the nevoid basal cell carcinoma syndrome) is a rare autosomal dominant syndrome caused due to mutations in the patched gene found on chromosome arm 9 q. It shows high penetrance and variable expressivity; is characterized by basal cell carcinomas, odontogenic keratocysts, palmar and/or plantar pits and ectopic ...
Mehta, DN +3 more
openaire +3 more sources
Gorlin syndrome - an incidental radiographic detection
South African Journal of Radiology, 2011 Gorlin-Goltz syndrome (also known as nevoid basal cell carcinoma syndrome) was first reported in 1894, but described by Gorlin and Goltz in 1960 as a distinct entity consisting of ectodermal and mesodermal abnormalities.
Shishir Ram Shetty +5 more
doaj +1 more source
Egyptian Journal of Medical Human Genetics, 2023 Background Gorlin syndrome (GS) is a rare genetic disorder inherited in an autosomal dominant manner caused by genetic variants in PTCH1, SUFU, or PTCH2 genes.
Paula Conde-Rubio +4 more
doaj +1 more source
Basal Cell Carcinomas in Gorlin Syndrome: A Review of 202 Patients
Journal of Skin Cancer, 2011 Gorlin syndrome (Naevoid Basal Cell Carcinoma Syndrome) is a rare autosomal dominant syndrome caused by mutations in the PTCH gene with a birth incidence of approximately 1 in 19,000. Patients develop multiple basal cell carcinomas of the skin frequently
Elizabeth A. Jones +3 more
doaj +1 more source
Basaloid follicular hamartoma associated with follicular mucinosis and inflammation
Anais Brasileiros de Dermatologia, 2022 Basaloid follicular hamartoma is a benign, superficial malformation of hair follicles that can be mistaken both clinical and histopathologically for basal cell carcinoma.
Solange Edelman +3 more
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Journal of Oral and Maxillofacial Pathology, 2009 Gorlin-Goltz syndrome is an autosomal dominant inherited disorder characterized by the presence of multiple odontogenic keratocysts along with various cutaneous, dental, osseous, ophthalmic, neurological, and sex organ abnormalities. Early diagnosis is essential as it may progress to aggressive basal cell carcinomas and neoplasias.
Jawa, Deepti Singh +5 more
openaire +3 more sources
Gorlin-Goltz syndrome: A rare case
Indian Journal of Dermatology, 2015 Gorlin-Goltz syndrome or nevoid basal cell carcinoma syndrome is characterized by multiple basocellular epitheliomas, keratocysts in the jaws, bifid ribs, palmar and/or plantar pits and ectopic calcifications of the falx cerebri.
Satyaki Ganguly +4 more
doaj +1 more source