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Gorlin Goltz syndrome: A clinicopathological case report
Journal of Indian Academy of Oral Medicine and Radiology, 2014 The Gorlin-Goltz syndrome is an infrequent multisystemic disease, which is inherited in an autosomal dominant manner. This shows a high level of penetrance and variable expressiveness, characterized by multiple basal cell nevi or carcinomas, odontogenic ...
Shobha C Bijjaragi +3 more
doaj +2 more sources
Gorlin-Goltz Syndrome: case report and review of literature [PDF]
Clinical and Biomedical Research, 2014 Description of a case report of Gorlin-Goltz Syndrome diagnosed in a male newborn who presented increased head circumference and bifid ribs. Mother and grandmother presented typical physical findings of the syndrome, including palmar pits, odontogenic ...
Adrianne Rahde Bischoff +6 more
doaj +8 more sources
A Case Report of Gorlin-goltz Syndrome
Journal of Contemporary Medical Sciences, 2016 Nevoid basal cell carcinoma syndrome (Gorlin syndrome) is an autosomal dominant inherited condition that exhibits high penetrance and variable expressivity.
Shima Nafarzadeh +2 more
doaj +1 more source
Gorlin-Goltz Syndrome: Diagnosis and Treatment Options [PDF]
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 +2 more sources
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
+6 more sources
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 +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
Gorlin-Goltz Syndrome and Neoplasms: A Case Study
, 2010 Gorlin syndrome is a rare autosomal dominant disorder exhibiting high penetrance and variable expressivity. It is characterized by facial dysmorphism, skeletal anomalies, multiple basal cell carcinomas, odontogenic keratocysts (OKC), palmar and plantar ...
Lee, Maria Lucia +5 more
core +5 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