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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
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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
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
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Gorlin Goltz syndrome: a rare case report [PDF]
, 2020 Gorlin-Goltz syndrome is uncommon multisystemic disease with an autosomal dominant trait, with complete penetrance and variable expressivity, though sporadic cases have been described.
Gandhi, Mily S. +3 more
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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
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
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Electrochemotherapy: a Valid Treatment for Gorlin Goltz syndrome [PDF]
, 2013 Gorlin-Goltz syndrome is a rare disorder, characterized by systemic manifestations included multiple basal cell carcinomas, palmar or plantar pits, odontogenic keratocysts and ectopic calcifications of the falx cerebri.
Calvieri, Stefano +4 more
core +1 more source
Tonsillar Hypertrophy in Goltz-Gorlin Syndrome: Case Report and Literature Review
B-ENT, 2023 Goltz-Gorlin syndrome, also known as focal dermal hypoplasia or nevoid basal cell carcinoma syndrome, is a rare multisystemic disease caused by autosomal dominant mutations in the PORCN gene.
Emilie Lavrysen +3 more
doaj +2 more sources