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2018
Basal cell carcinoma syndrome, also known as Gorlin-Goltz syndrome, is an autosomal-dominant disease characterized by multiple basal cell carcinomas (BCCs) since childhood along with other multiorgan abnormalities. Pigmented and non-pigmented BCC and palmar pits are often small and hardly visible to the naked eye.
Iria Neri, Neri Iria
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Basal cell carcinoma syndrome, also known as Gorlin-Goltz syndrome, is an autosomal-dominant disease characterized by multiple basal cell carcinomas (BCCs) since childhood along with other multiorgan abnormalities. Pigmented and non-pigmented BCC and palmar pits are often small and hardly visible to the naked eye.
Iria Neri, Neri Iria
exaly +4 more sources
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
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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
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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 ...
Ching-Wan Lam +2 more
exaly +2 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
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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
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International Journal of Oral Surgery, 1979
T. Nakajima, T. Yokobayashi, M. Onishi
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T. Nakajima, T. Yokobayashi, M. Onishi
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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
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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
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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
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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
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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
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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
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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
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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
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