Results 91 to 100 of about 7,017,185 (188)

Nevoid Basal-cell Syndrome: Literature Review And Case Report In A Family. [PDF]

open access: yes, 2015
The Nevoid Basal-Cell Carcinoma Syndrome (NBCC), or as it is also referred to, basal-cell nevus syndrome or Gorlin-Goltz syndrome, is characterized by multiple early-appearing basal cell carcinomas, keratocytosis of the mandible, and anomalies of the ...
Franco Mello Jr. E.J.   +4 more
core  

A Case Report of Gorlin-goltz Syndrome

open access: yesJournal 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  

The role of GLI2 in human basal cell carcinoma tumourigenesis [PDF]

open access: yes, 2010
PhDAbnormal Sonic Hedgehog (SHH) signalling leads to increased transcriptional activation of its downstream effector, GLI2, which is implicated in the pathogenesis of a variety of human tumours, including human basal cell carcinoma (BCC).
Pantazi, Eleni
core   +1 more source

Gorlin-Goltz Syndrome: Case Report of a Rare Hereditary Disorder

open access: yesCase Reports in Dentistry, 2012
Introduction. Gorlin-Goltz syndrome is an inherited autosomal dominant disorder with complete penetrance and extreme variable expressivity. Case Report.
Ashutosh Agrawal   +3 more
doaj   +1 more source

Nevoid Basal Cell Carcinoma Syndrome.

open access: yesIndian journal of dermatology, venereology and leprology, 2017
A 65 years old male developed nevoid basal cell carcinoma syndrome, manifesting as multiple basal cell epitheliomas, marked mutilation of the face and characteristic pitting on the palms and soles. Calcification of the falx cerebri and scoliosis of the lumbar spine were also seen.
F, Handa   +2 more
openaire   +1 more source

Genetic Insight into Gorlin–Goltz Syndrome

open access: yesIndian Journal of Dermatology
Gorlin-Goltz syndrome, also called Basal cell nevus syndrome (BCNS), Nevoid basal cell carcinoma syndrome (NBCCS), or Basal nevus cell carcinoma syndrome (BNCCS) is a rare, inherited, autosomal dominant genodermatoses, with variable expression and ...
M Madhu
doaj   +1 more source

Calcified ovarian fibroma presentation in nevoid basal cell carcinoma syndrome. [PDF]

open access: yesRep Pract Oncol Radiother, 2022
Al Khatalin M   +4 more
europepmc   +1 more source

Non-Syndromic Recurrent Multiple Odontogenic Keratocysts: A Case Report

open access: yesFrontiers in Dentistry, 2011
Odontogenic keratocysts (OKCs) are one of the most frequent features of nevoid basal cell carcinoma syndrome (NBS). It is linked with mutation in the PTCH gene. Partial expression of the gene may result in occurrence of only multiple recurring OKC.
AR. Bartake   +3 more
doaj  

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