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Tumor burden and management of basal cell carcinoma in Korean patients with Gorlin syndrome. [PDF]
JAAD IntSupplemental data for the article entitled "Tumor Burden and Management of Basal Cell Carcinoma in Korean Patients with Gorlin ...
Lee J +7 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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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
Frontiers in Oncology, 2020 The nevoid basal cell carcinoma syndrome (NBCCS), also called Gorlin syndrome is an autosomal dominant disorder whose incidence is estimated at about 1 per 55,600–256,000 individuals.
Aurélie Charazac +16 more
doaj +1 more source
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
Multi-layered mutation in hedgehog-related genes in Gorlin syndrome may affect the phenotype. [PDF]
PLoS ONE, 2017 Gorlin syndrome is a genetic disorder of autosomal dominant inheritance that predisposes the affected individual to a variety of disorders that are attributed largely to heterozygous germline patched1 (PTCH1) mutations.
Shoko Onodera +9 more
doaj +1 more source
Orphanet Journal of Rare Diseases, 2015 Meier-Gorlin syndrome (MGS) is a rare autosomal recessive primordial dwarfism disorder, characterized by microtia, patellar applasia/hypoplasia, and a proportionate short stature. Associated clinical features encompass feeding problems, congenital pulmonary emphysema, mammary hypoplasia in females and urogenital anomalies, such as cryptorchidism and ...
de Munnik, Sonja A +7 more
openaire +6 more sources
Gorlin Syndrome in Eleven Patients [PDF]
, 2017 Aim: Gorlin syndrome is an autosomal dominant disorder characterized by cutaneous basal cell carcinomas, odontogenic keratocysts and skeletal anomalies. Predisposition to certain types of cancers is among the main features of the disease.
TUNÇBİLEK, ERGÜL +11 more
core +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
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