Results 61 to 70 of about 1,019 (146)
Journal of Ophthalmology, Volume 2024, Issue 1, 2024.Purpose. Basal cell carcinoma (BCC) is the most frequent malignant periocular tumor. It is associated with exposure to ultraviolet radiation, and its incidence is gradually increasing. It may occasionally display more aggressive behavior and result in orbital or intracranial invasion. Mortality from periocular BBC with orbital invasion is very low, but
Alvaro Bengoa-González +5 more
wiley +1 more source
Gorlin-Goltz Syndrome: Diagnosis and Treatment Options
Acta Médica Portuguesa, 2017 The Gorlin-Goltz syndrome is a rare autosomal dominant hereditary condition, with complete penetrance and variable expressivity. Characterized by the appearance of multiple basaliomas, and often the development of keratocyst, it can also express itself ...
João Mendes-Abreu +4 more
doaj +1 more source
Ankara Universitesi Dis Hekimligi Fakultesi dergisi = The Journal of the Dental Faculty of Ankara University, 1991 Gorlin-Goltz syndrome has mainly three components; basal cell carcinoma, jaw cysts and skeletal anomalies. However, various cases of this syndrome with over 40 different kinds of components have been reported. In this paper, a case with Gorlin-Goltz syndrome treated in our clinic have been presented and discussed.
K, Sevin, N, Kutlu, M O, Yenidünya
openaire +3 more sources
Jaw cyst-Basal cell nevus-Bifid rib syndrome: A case report
Journal of Indian Society of Pedodontics and Preventive Dentistry, 2007 Jaw cyst-Basal cell nevus-Bifid rib syndrome or Gorlin-Goltz syndrome involves multiple organ system. The most common findings include multiple odontogenic keratocysts in the jaws and basal cell nevus on the skin that have an early age onset.
Rai S, Gauba K
doaj
THE EXPERIENCE OF TREATMENT OF MULTIPLE BASALIOMA IN GORLIN-GOLTZ SYNDROME
Alʹmanah Kliničeskoj Mediciny, 2016 Aim: To assess clinical efficacy of the treatment options for multiple basalioma in patients with Gorlin-Goltz syndrome. Materials and methods: We retrospectively analyzed the results of various treatments in 23 patients with the Gorlin-Goltz syndrome ...
E. I. Tret'yakova
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JDDG: Journal der Deutschen Dermatologischen Gesellschaft, Volume 22, Issue 3, Page 434-437, March 2024.
Ines Bertlich +5 more
wiley +1 more source
A case report of Gorlin-Goltz syndrome as a rare hereditary disorder
Journal of Research in Medical Sciences, 2011 Gorlin-Goltz syndrome is an autosomal dominant and a rare hereditary disease. Diagnosis of this syndrome is based on major and minor criteria. We report a Gorlin-Goltz syndrome in a 25-year-old male who was presented with progressive pain of maxilla and ...
Mehri Sirous, Nazila Tayari
doaj
The Gorlin-Goltz syndrome: a sporadic case
Pan African Medical Journal, 2014 Gorlin-Goltz syndrome, also known as basal cell nevus syndrome, is an uncommon autosomal dominant hereditary disorder; which is characterized by numerous basal cell carcinomas, maxillary keratocysts and bones malformations. It results from a mutation of the PATCHED gene. The estimate incidence for a general population is 1/50000 to 1/150000. We present
Kawtar Inani, Fatimazahra Mernissi
openaire +3 more sources
Gorlin-Goltz Syndrome: A Case Series. [PDF]
Cureus, 2023 Salahudheen A +4 more
europepmc +1 more source
Gorlin-Goltz Syndrome: Report of a Rare Case with an Update on the Review of the Literature. [PDF]
Contemp Clin Dent, 2023 Attur S, Patel JK, Attur K, Menat S.
europepmc +1 more source