Results 1 to 10 of about 5,064 (152)
Indian Journal of Dermatology, 2013 Gorlin Syndrome, a rare genodermatosis, otherwise known as Nevoid basal cell carcinoma syndrome (NBCCS) is a multisystem disease affecting skin, nervous system, eyes, endocrine glands, and bones.
Basanti Devi +4 more
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Dental Research Journal, 2012 Gorlin-Goltz syndrome is an uncommon autosomal dominant inherited disorder, which is characterized by multiple odontogenic Keratocysts and basal cell carcinomas, skeletal, dental, ophthalmic, and neurological abnormalities, intracranial ectopic ...
Priya Shirish Joshi +2 more
doaj +6 more sources
Nevoid basal cell carcinoma syndrome (Gorlin syndrome): a case report [PDF]
Journal of Medical Case ReportsBackground Basal cell nevus syndrome, also known as Gorlin or Gorlin–Goltz syndrome, is a hereditary condition caused by mutation in the PATCHED gene.
Noura Abdul Rahman +4 more
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Journal of Indian Academy of Oral Medicine and Radiology, 2010 Gorlin-Goltz syndrome, also known as basal cell nevus syndrome, is an uncommon autosomal dominant inherited disorder characterized by numerous basal cell carcinomas, odontogenic keratocysts, and musculoskeletal malformation. It is occasionally associated
M K Sunil +3 more
doaj +4 more sources
Gorlin Syndrome: A Comprehensive Evaluation of Skin Findings [PDF]
Turkish Archives of PediatricsObjective: Although Gorlin syndrome has rich skin findings, there is limited information about their subtypes, features specific to this genodermatosis, and relationships with each other.
Tuğba Atcı +2 more
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Journal of Indian Academy of Oral Medicine and Radiology, 2011 Gorlin-Goltz syndrome also known as nevoid basal cell carcinoma syndrome (NBCCS) is an infrequent multisystemic disease inherited in a dominant autosomal way, which shows a high level of penetrance and variable expressiveness.
B V Shobha +5 more
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Surgical management of ovarian fibromas in young patients with Gorlin syndrome: a case series and review of the literature [PDF]
F&S ReportsObjective: To characterize the presentation and surgical management of ovarian fibromas among a case series of pediatric and adolescent patients with Gorlin syndrome. Design: Retrospective case series. Setting: Tertiary-care hospital.
Danielle T. Cipres, M.D. +1 more
doaj +2 more sources
Novel alterations in IFT172 and KIFAP3 may induce basal cell carcinoma
Orphanet Journal of Rare Diseases, 2021 Background Basal cell carcinoma (BCC) is the most commonly occurring neoplasm in patients with Gorlin syndrome. It is widely accepted that multiple basal cell carcinomas simultaneously develop in middle-aged patients with this syndrome.
Shoko Onodera +8 more
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Gorlin–Goltz syndrome and epilepsy: A two-case report and review of the literature
Epilepsy & Behavior Reports, 2020 Gorlin–Goltz syndrome, also known as nevoid basal cell carcinoma syndrome, is a genetic disorder with several neurological, cutaneous and skeletal manifestations. Epilepsy has been previously reported as a finding in Gorlin–Goltz syndrome but remains ill-
Daniel Tomasso +2 more
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Gorlin-Goltz syndrome from diagnosis to treatment: Role of the dentist
Advances in Oral and Maxillofacial Surgery, 2023 Gorlin-Goltz syndrome encompasses a variety of clinical signs and symptoms, including significant oral manifestations of which dentists should be aware. Given the risk of malignancy, it is important to be aware of this syndrome and recognize the need for
Basma Zaher +2 more
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