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Basal cell nevus syndrome

Archives of Medicine and Health Sciences, 2021
Gorlin-Goltz syndrome (GGS) is a hereditary condition; it is transmitted as an autosomal dominant trait and characterized by a wide range of developmental abnormalities and a tendency to neoplasm.
Anjali Ravi, Hannah Maryam Mohiddin, Bhargabi Paul Majumder, Vishal S Nair, Y R Girish, Prasanna Kumar Rao, Deepak Pai, Raghavendra Kini, Nitin Gonsalves   +8 more
doaj   +2 more sources

Calcified ovarian fibromas complicated with basal cell nevus syndrome [PDF]

Gynecology and Minimally Invasive Therapy, 2021
Basal cell nevus syndrome (BCNS) is a rare neurocutaneous syndrome characterized by tumorigeneses such as basal cell carcinomas, jaw cysts, ovarian fibromas, and cardiac fibromas. We present a 24-year-old female with calcified ovarian fibromas associated
Daiken Osaku, Fuminori Taniguchi, Hiroaki Komatsu, Hermawan Wibisono, Yukihiro Azuma, Tasuku Harada   +5 more
doaj   +2 more sources

Basal Cell Nevus Syndrome and Sporadic Basal Cell Carcinoma: A Comparative Study of Clinicopathological Features [PDF]

Acta Dermato-Venereologica
Basal cell nevus syndrome is caused by mutations in the Sonic hedgehog pathway and characterized by early-onset basal cell carcinoma. The features of basal cell carcinoma in basal cell nevus syndrome compared with sporadic basal cell carcinoma have not ...
Ching-Ya Wang, Chun-Bing Chen, Franchesca Marie D. Ilagan, Jing-Yi Lin, Wen-Yi Sung, Lai-Ying Lu, Jau-Yu Liau, Yu-Hsiu Chen, Yi-Hua Liao, Jau-Shiuh Chen, Yi-Shuan Sheen, Yao-Yu Chang, Jin-Bon Hong   +12 more
doaj   +2 more sources

Panfolliculoma in SUFU-mutated basal cell nevus syndrome [PDF]

JAAD Case Reports, 2023
Areeba Abid, BS, Douglas Parker, MD, Travis W. Blalock, MD   +2 more
doaj   +2 more sources

Detection of PTCH1 Copy-Number Variants in Mosaic Basal Cell Nevus Syndrome [PDF]

Biomedicines
Basal cell nevus syndrome (BCNS) is an inherited disorder characterized mainly by the development of basal cell carcinomas (BCCs) at an early age. BCNS is caused by heterozygous small-nucleotide variants (SNVs) and copy-number variants (CNVs) in the ...
Guido M. J. M. Roemen, Tom E. J. Theunissen, Ward W. J. Hoezen, Anja R. M. Steyls, Aimee D. C. Paulussen, Klara Mosterd, Elisa Rahikkala, Axel zur Hausen, Ernst Jan M. Speel, Michel van Geel   +9 more
doaj   +2 more sources

Genetic Insight into Gorlin–Goltz Syndrome

Indian 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   +2 more sources

Basaloid follicular hamartomas in pediatric Basal Cell Nevus Syndrome: A diagnostic challenge. [PDF]

J Dermatol, 2021
Besagni F, Dika E, Ricci C, Misciali C, Veronesi G, Corti B, Gurioli C, Neri I.   +7 more
europepmc   +2 more sources

Vismodegib-resistant basal cell carcinomas in basal cell nevus syndrome: Clinical approach and genetic analysis. [PDF]

JAAD Case Rep, 2018
Sinx KAE, Roemen GMJM, van Zutven V, Janssen R, Speel EM, Steijlen PM, van Geel M, Mosterd K.   +7 more
europepmc   +2 more sources

Inhibiting the hedgehog pathway in patients with the basal-cell nevus syndrome. [PDF]

N Engl J Med, 2012
Tang JY, Mackay-Wiggan JM, Aszterbaum M, Yauch RL, Lindgren J, Chang K, Coppola C, Chanana AM, Marji J, Bickers DR, Epstein EH.   +10 more
europepmc   +2 more sources

BASAL CELL NEVUS SYNDROME [PDF]

American Journal of Roentgenology, 1968
The manifestations of an inherited syndrome with emphasis on the roentgenographic findings have been described. Thirteen additional cases are reported and an example of extensive involvement of one family is presented. The importance of recognition of this syndrome, especially in children, because of the malignant potential and the need for genetic ...
C J, Rater, A C, Selke, E F, Van Epps
openaire   +2 more sources