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Gorlin Goltz Syndrome- A Rare Disease Reported In Bangladesh
Update Dental College Journal, 2022 Gorlin-Goltz syndrome is an infrequent multisystemic disease with an autosomal dominant trait with complete penetrance and various expressivity. Gorlin Goltz Syndrome is a rare autosomal characterized by an increased predisposition to basal cell ...
Nafisa Afroze +3 more
doaj +1 more source
Klinicka Onkologie, 2019 Gorlin-Goltz syndrome is an autosomal dominant inherited disorder characterized by a predisposition to various cancers. Clinicopathological findings of syndrome are very diverse and many symptoms begin to manifest in a certain period of life.The authors describe a case report of a man who, at the age of 34 years, presented to a dermatologist with ...
V, Bartoš +3 more
openaire +2 more sources
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
+6 more sources
Case report: Sequential treatment strategy for advanced basal cell carcinoma in Gorlin-Goltz syndrome: integration of vismodegib, radiotherapy, surgery, and high-intensity focused ultrasound [PDF]
Frontiers in OncologyNatalia Sauer
exaly +2 more sources
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
Journal of the College of Physicians and Surgeons--Pakistan : JCPSP, 2015 A 12 years old girl was presented with bilateral swellings on angle and body of mandible. On general physical examination, there were polydactyly and papular lesions on arm. Histopathology of mandibular lesions revealed odontogenic keratocysts. Marsupialization of the cysts followed by enucleation was done. The patient was reviewed every six months and
Ali Akhtar, Khan +3 more
+9 more sources
Indian Journal of Pathology and Microbiology, 2011 Nevoid cell carcinoma syndrome or Gorlin-Goltz syndrome is an autosomal dominant disorder characterized by multiple basal cell carcinoma, multiple keratocyst tumors, and skeletal anomalies.
Cláudio M Pereira +4 more
doaj +1 more source
King Khalid University Journal of Health Sciences, 2016 Gorlin-Goltz syndrome is an autosomal dominant inherited syndrome. It is also known as hereditary cutaneo-mandibular polyonocosis, multiple nevoid basal cell epithelioma-jaw cysts or bifid rib syndrome.
Nasser Alasseri +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
doaj +1 more source
Appearance and recurrence of odontogenic keratocysts
Clinical and Experimental Dental Research, Volume 9, Issue 5, Page 894-898, October 2023., 2023 Abstract Objective The purpose of this study was to evaluate the appearance, histopathological features, and recurrence of odontogenic keratocysts (OKCs) from a large single institute registry over a 36‐year period. Materials and Methods A total of 226 cases of OKC were identified in 174 patients over a 36‐year period in a single institute in ...
Jaakko Pylkkö +4 more
wiley +1 more source