Results 81 to 90 of about 7,017,185 (188)

A Rare Case of a Symptomatic Tumor Found in the Groin Area: An Atypical Location Unexposed to the Known Causes

Case Reports in Oncology, 2015
Nevoid basal cell carcinoma syndrome (NBCCS), also known as Gorlin syndrome, is a rare hereditary condition characterized by a wide range of developmental abnormalities and a predisposition to neoplasms.
Ellen Toyonaga, Hiroo Hata, Chihiro Nakayama, Erina Homma, Toshiyuki Miyashita, Hiroshi Shimizu   +5 more
doaj   +1 more source

A Novel PTCH1 Frameshift Mutation Leading to Nevoid Basal Cell Carcinoma Syndrome [PDF]

, 2018
Nevoid basal cell carcinoma syndrome (NBCCS), also known as Gorlin syndrome, is a rare multisystemic autosomal dominant disorder typically presenting with cutaneous basal cell carcinomas, multiple keratocysts, and skeletal anomalies.
Pelin Ertop, Ertop, Pelin, Miriam J. Smith, Durmaz, Ceren D., Evans, D Gareth; id_orcid, Smith, Miriam J; id_orcid, Akay, Bengü N., Gareth Evans, Bengü N. Akay, Timur Tuncalı, Ceren D. Durmaz, AKAY, BÜLENT, Smith, Miriam J., TUNCALI, TİMUR, Durmaz, CEREN DAMLA, Evans, Gareth   +15 more
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Gorlin-goltz syndrome

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, S Mosby, N Barkha, Biswajeet, M Ajit, T Deepak   +5 more
doaj   +1 more source

A Rare Case of Gorlin-Goltz Syndrome in Children

Case Reports in Dentistry, 2019
The Gorlin-Goltz syndrome, nevoid basal cell carcinoma syndrome, or basal cell nevus syndrome is an autosomal dominant condition disorder with high variability expression.
Fernanda Brasil Daura Jorge Boos Lima, Ana Paula Cota Viana, Luciano Henrique Ferreira Lima, Bruna Campos Ribeiro, Carlos Eduardo Assis Dutra, Glaykon Alex Vitti Stabile, Sergio Monteiro Lima Junior   +6 more
doaj   +1 more source

Basal Cell Carcinoma of the Buccal Mucosa in a Patient with Nevoid Basal Cell Carcinoma Syndrome

, 2011
Basal cell carcinoma (BCC) of the oral cavity is a controversial lesion with clinical and histopathologic features that overlap with those of peripheral ameloblastoma (PA). Ber-EP4, a cell surface glycoprotein preferentially expressed in BCC of the skin,
Allen, Carl M., Rawal, Yeshwant B., Kalmar, John R., Shumway, Brian S.   +3 more
core   +1 more source

Gorlin syndrome - an incidental radiographic detection

South African Journal of Radiology, 2011
Gorlin-Goltz syndrome (also known as nevoid basal cell carcinoma syndrome) was first reported in 1894, but described by Gorlin and Goltz in 1960 as a distinct entity consisting of ectodermal and mesodermal abnormalities.
Shishir Ram Shetty, K M Veena, Laxmikanth Chatra, Prashanth Shenai, Prasanna Kumar Rao, Jagadish Chandra   +5 more
doaj   +1 more source

Spectrum of PTCH mutations in Italian nevoid basal cell-carcinoma syndrome patients: identification of thirteen novel alleles

, 2004
The nevoid basal cell carcinoma syndrome (NBCCS) is an autosomal dominant genetic disease characterized by numerous basal cell carcinomas, odontogenic keratocysts of the jaws, palmar and plantal pits, skeletal abnormalities, and calcification of the falx
RENIERI A., FORMICA V., DAPOLITO M, DALLAPICCOLA B., ANDREUCCI E., SAVOIA A., MARI F., SAVINO M, LO MUZIO L, CARABBA E., LO MUZIO L., LO MUZIO, LORENZO, FORMICA V, TARANTINO E, BELLI B, SAVOIA, ANNA, ZELANTE L., RENIERI A, DALLAPICCOLA B, BELLI S., SAVINO M., ANDREUCCI E, TARANTINO E., MARI F, BAORDA F., BAORDA F, D'APOLITO M, BELLI S, D'APOLITO M., CARABBA E, ZELANTE L   +30 more
core   +1 more source

Gorlin Syndrome in a type IV-skin person with a novel PTCH1 mutation: Case report and literature review

Journal of Dermatology and Dermatologic Surgery, 2016
Nevoid basal cell carcinoma syndrome (NBCCS), or Gorlin Syndrome, is an autosomal dominant multisystem disorder, characterized by multiple developmental abnormalities and inactivation germline mutations in the human homolog of the patched (PTCH) gene. We
S. AlSalem, Y. Binamer
doaj   +1 more source

Non-syndromic multiple keratocyst odontogenic tumor: A rare case report

Journal of Indian Academy of Oral Medicine and Radiology, 2015
Keratocystic odontogenic tumors (KCOTs) are one of the most frequent features of nevoid basal cell carcinoma syndrome (NBCCS). The condition is linked with mutation in the PTCH gene.
Abhijeet Alok, Sunil R Panat, Indra Deo Singh, Shivani Singh   +3 more
doaj   +1 more source

Gorlin syndrome associated with basal cell carcinoma of the vulva: a case report

, 2006
Gorlin syndrome, also known as nevoid basal cell carcinoma syndrome (NBCCS), is a hereditary condition transmitted as an autosomal dominant trait with high penetrance and variable expressivity.
DI STEFANO, LEONARDO, MASCARETTI, Giulio, LEOCATA, Pietro, ZOCCALI, GIOVANNI, Angelone, E, GIULIANI, Maurizio   +5 more
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