Results 151 to 160 of about 6,707,637 (199)
Some of the next articles are maybe not open access.
Archives of Dermatology, 1964
The basal cell nevus syndrome is hereditary with multiple defects involving organs and systems of both ectodermal and mesodermal origin. While the major components of the syndrome (basal cell epitheliomas, mandibular cysts, minor rib anomalies) are well recognized, there are a number of less constant defects which merit attention and further study ...
W E, CLENDENNING, J B, BLOCK, I G, RADDE
openaire +3 more sources
The basal cell nevus syndrome is hereditary with multiple defects involving organs and systems of both ectodermal and mesodermal origin. While the major components of the syndrome (basal cell epitheliomas, mandibular cysts, minor rib anomalies) are well recognized, there are a number of less constant defects which merit attention and further study ...
W E, CLENDENNING, J B, BLOCK, I G, RADDE
openaire +3 more sources
Current Opinion in Oncology, 2005
Basal cell nevus syndrome (BCNS), is a hereditary condition transmitted as an autosomal dominant trait exhibiting high penetrance and variable expressivity. Inherited or spontaneous mutations in the human homologue of the Drosophila patched gene underlie the disorder and in addition to tumor predisposition, are associated with a range of 'patterning ...
Alec, High, Walid, Zedan
openaire +2 more sources
Basal cell nevus syndrome (BCNS), is a hereditary condition transmitted as an autosomal dominant trait exhibiting high penetrance and variable expressivity. Inherited or spontaneous mutations in the human homologue of the Drosophila patched gene underlie the disorder and in addition to tumor predisposition, are associated with a range of 'patterning ...
Alec, High, Walid, Zedan
openaire +2 more sources
JAMA, 1964
The basal cell nevus syndrome is a hereditary affection characterized primarily by multiple genetically determined basal cell carcinomas, cysts of the jaws, peculiar pits of the hands and feet, and developmental anomalies of the ribs, spine, and skull. These, as well as other associated anomalies, serve to differentiate the nevoid basal cell carcinoma ...
J B, HOWELL +2 more
openaire +2 more sources
The basal cell nevus syndrome is a hereditary affection characterized primarily by multiple genetically determined basal cell carcinomas, cysts of the jaws, peculiar pits of the hands and feet, and developmental anomalies of the ribs, spine, and skull. These, as well as other associated anomalies, serve to differentiate the nevoid basal cell carcinoma ...
J B, HOWELL +2 more
openaire +2 more sources
American Journal of Roentgenology, 1968
1. Four cases of the basal cell nevus syndrome occurring within a single family are described.2. The patients show many of the characteristic roentgen findings of the syndrome including mandibular cysts, calcification of the falx cerebri, vertebral anomalies, rib anomalies, and brachymetacarpalism.3.
H A, Lile, J F, Rogers, B, Gerald
openaire +2 more sources
1. Four cases of the basal cell nevus syndrome occurring within a single family are described.2. The patients show many of the characteristic roentgen findings of the syndrome including mandibular cysts, calcification of the falx cerebri, vertebral anomalies, rib anomalies, and brachymetacarpalism.3.
H A, Lile, J F, Rogers, B, Gerald
openaire +2 more sources
Plastic and Reconstructive Surgery, 1977
We report two patients with basal cell nevus syndrome. They had two previously unreported associated conditions--a myocardial fibroma and bilateral basal cell carcinomas of the soles of the feet. The syndrome is discussed, the literature is reviewed, and the management is outlined.
P D, Bunting, J P, Remensnyder
openaire +2 more sources
We report two patients with basal cell nevus syndrome. They had two previously unreported associated conditions--a myocardial fibroma and bilateral basal cell carcinomas of the soles of the feet. The syndrome is discussed, the literature is reviewed, and the management is outlined.
P D, Bunting, J P, Remensnyder
openaire +2 more sources
Basal Cell Nevus Syndrome or Gorlin Syndrome
Handbook of Clinical Neurology / Edited By P J Vinken and G W Bruyn, 2015Basal cell nevus syndrome (BCNS) or Gorlin syndrome is a rare neurocutaneous syndrome sometimes known as the fifth phacomatosis, inherited in autosomal dominant fashion with complete penetrance and variable expressivity. Gorlin syndrome is characterized by development of multiple basal cell carcinomas (BCCs), jaw cysts, palmar or plantar pits ...
Srikanth, Thalakoti, Thomas, Geller
exaly +3 more sources
Gorlin's Basal Cell Nevus Syndrome
Archives of Otolaryngology - Head and Neck Surgery, 1986A case report is used to illustrate the characteristics of Gorlin's syndrome and to emphasize the need for early recognition by the physician and for thorough lifetime follow-up by the patient to prevent severe sequelae.
S C, Owens +4 more
openaire +2 more sources
Dermatologica, 2009
A single patient with basal cell nevus syndrome is presented. Prolonged application of 5% 5-fluorouracil and dinitrochlorobenzene was unsuccessful in inducing regression or clearing of his cutaneous lesions. Our results suggest that these therapies, at least for the nevoid-appearing lesions, may not be effective in the management of some patients with ...
Paul G. Hazen, Steven J. Taub
openaire +2 more sources
A single patient with basal cell nevus syndrome is presented. Prolonged application of 5% 5-fluorouracil and dinitrochlorobenzene was unsuccessful in inducing regression or clearing of his cutaneous lesions. Our results suggest that these therapies, at least for the nevoid-appearing lesions, may not be effective in the management of some patients with ...
Paul G. Hazen, Steven J. Taub
openaire +2 more sources
Novel Mutations in the PATCHED Gene in Basal Cell Nevus Syndrome
Molecular Genetics and Metabolism, 2002 Basal cell nevus syndrome (BCNS) is an autosomal dominant disease characterized by the presence of multiple basal cell carcinomas, odontogenic keratocysts, palmoplantar pits, and calcification in the falx cerebri caused by mutational inactivation of the ...
Jingwu Xie, Ching-Wan Lam, Sui-Fan Tong
exaly +2 more sources
Familial basal cell nevus syndrome
Human Genetics, 1978The basal cell nevus syndrome is characterized by multiple basal cell nevi and basal cell carcinoma, cysts of the jaw, anomalies of ribs and spine, abnormal calcifications, and additional anomalies of the facial skull. A German family is described with manifestations of the syndrome in the mother and her three daughters.
R, Lorenz, W, Fuhrmann
openaire +2 more sources