Results 71 to 80 of about 1,573 (165)

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, Fatemeh Mozaffari, Oveis Khakbaz   +2 more
doaj  

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

Case 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, Aditi Murari, Sunil Vutukuri, Arun Singh   +3 more
doaj   +1 more source

Early diagnosis of Gorlin-Goltz syndrome: case report

Head & Face Medicine, 2011
The 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.
Trento Cleverson L, Veltrini Vanessa C, Moreschi Eduardo, Rocha Loures Daniela CN, Casaroto Ana R, Gottardo Vilmar D, Lara Vanessa S   +6 more
doaj   +1 more source

Nevoid Basal Cell Carcinoma Syndrome : A Case Report

Journal of Indian Academy of Oral Medicine and Radiology, 2004
The nevoid basal cell carcinoma syndrome (NBCCS) or Gorlin - Goltz syndrome is an autosomal disorder principally characterized by cutaneous basal cell carcinomas, multiple keratocysts, and skeletal anomalies.
K Rajanikanth, Satish Karandikar, Anisha Maria   +2 more
doaj  

Understanding Nevoid Basal Cell Carcinoma Syndrome (Gorlin Syndrome): A Case Report. [PDF]

Cureus, 2023
Olivero Y, Otero-Colón J, Rahman S, Grodman B, Vas V.   +4 more
europepmc   +1 more source

Radiological evaluation of odontogenic keratocysts in patients with nevoid basal cell carcinoma syndrome: A review. [PDF]

Saudi Dent J, 2023
Ünsal G, Cicciù M, Ayman Ahmad Saleh R, Riyadh Ali Hammamy M, Amer Kadri A, Kuran B, Minervini G.   +6 more
europepmc   +1 more source

Non-Syndromic Recurrent Multiple Odontogenic Keratocysts: A Case Report

Frontiers 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, NG. Shreekanth, Prabhu, K. Gopalkrishnan   +3 more
doaj  

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

Rep Pract Oncol Radiother, 2022
Al Khatalin M, Alzu'bi AY, Elwakil M, Camurdan VB, Yildirim O.   +4 more
europepmc   +1 more source

Tolerance of sonidegib after intolerance of vismodegib-Experience in two patients with nevoid basal cell carcinoma syndrome (Gorlin syndrome). [PDF]

Skin Health Dis, 2023
Venturi F, Trane L, Silvestri F, Zuccaro B, Magnaterra E, De Giorgi V.   +5 more
europepmc   +1 more source

Standard Poster Abstracts for the 17th Asia Pacific Heart Rhythm Society (APHRS) Scientific Sessions

Journal of Arrhythmia, Volume 41, Issue 2, April 2025.
wiley   +1 more source