Results 11 to 20 of about 7,017,185 (188)
Nevoid basal cell carcinoma syndrome
Indian Journal of Dental Research, 2006 Binkley and Johnson first reported this syndrome in 1951. But it was in 1960, Gorlin-Goltz established the association of basal cell epithelioma, jaw cyst and bifid ribs, a combination which is now frequently known as Gorlin-Goltz syndrome as well as ...
Kannan Karthiga +2 more
doaj +4 more sources
Two male patients with nevoid basal cell carcinoma syndrome from Turkey
The Turkish Journal of Pediatrics, 2001 Nevoid basal cell carcinoma syndrome, also known as Gorlin's syndrome, is a familial autosomal dominant syndrome characterized by multiple basal cell carcinomas, multiple odontogenic keratocysts of the jaws, and skeletal anomalies. Both tumors and
C Tümer, N Er, S Balci, A Ataç
doaj +4 more sources
Nevoid Basal-Cell Carcinoma (Gorlin) Syndrome
Pediatric Neurology Briefs, 1996 A unique case of a 15-year-old girl with nevoid basal-cell carcinoma (NBCCS), who presented with uncontrolled temporal lobe epilepsy due to neuronal heterotopia, is reported from the Royal Melbourne Hospital, Australia.
J Gordon Millichap
doaj +2 more sources
Nevoid basal cell carcinoma syndrome (Gorlin-Goltz syndrome)
Contemporary Clinical Dentistry, 2012 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.
N K Kiran +3 more
doaj +2 more sources
Nevoid basal cell carcinoma syndrome (Gorlin syndrome) [PDF]
Orphanet Journal of Rare Diseases, 2008 Nevoid basal cell carcinoma syndrome (NBCCS), also known as Gorlin syndrome, is a hereditary condition characterized by a wide range of developmental abnormalities and a predisposition to neoplasms.
Lo Muzio Lorenzo
doaj +3 more sources
Nevoid basal cell carcinoma syndrome: A case report
Pifu-xingbing zhenliaoxue zazhiA case of nevoid basal cell carcinoma syndrome is reported. A 47-year-old woman presented with a 10-year history of widespread asymptomatic nodules. Dermatological examination showed multiple hyperpigmented nodules and papules on the face, trunk, and ...
ZHONG Huiting +5 more
doaj +2 more sources
Exploration of the causative gene in a case of multiple nevoid basal cell carcinoma: A case report
Rare TumorsNevoid basal cell carcinoma syndrome is a rare autosomal dominant disorder characterized by a diverse clinical presentation, which includes developmental abnormalities and tumorigenesis that can impact multiple organ systems.
Yutong Liu +5 more
doaj +2 more sources
Nevoid basal cell carcinoma syndrome—case report and genetic study
Journal of Dental Sciences, 2010 Nevoid basal cell carcinoma syndrome (also named Gorlin-Goltz syndrome) is a rare disease. Commonly seen features include multiple odontogenic keratocysts (OKCs), nevus-like basal cell carcinoma, and bifid ribs.
Yu-Feng Huang +2 more
doaj +2 more sources
Nevoid basal cell carcinoma syndrome: A case report
Journal of Dr. NTR University of Health Sciences, 2018 Nevoid basal cell carcinoma syndrome (NBCCS) is an autosomal dominant inherited condition that exhibits high penetrance and variable expressivity. The syndrome is caused by mutations in patch (PTCH), a tumor suppressor gene that has been mapped to ...
Venkatesh K Dodda +3 more
doaj +2 more sources
Nevoid Basal-Cell Syndrome: literature review and case report in a family
São Paulo Medical JournalThe 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 ...
Alfio José Tincani +4 more
doaj +2 more sources