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Basal cell nevus syndrome or Gorlin syndrome
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
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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
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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
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2020
Basal cell nevus syndrome (BCNS) is a rare syndrome linked to mutations in the tumor suppressor gene PTCH and inherited in an autosomal dominant pattern, Its systemic manifestations include multiple basal cell carcinomas, keratocysts of the jaw, palmar and/or plantar pits, spine and rib anomalies, and calcification of the falx cerebri. The challenge in
Priyanka Chhadva, Pete Setabutr
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Basal cell nevus syndrome (BCNS) is a rare syndrome linked to mutations in the tumor suppressor gene PTCH and inherited in an autosomal dominant pattern, Its systemic manifestations include multiple basal cell carcinomas, keratocysts of the jaw, palmar and/or plantar pits, spine and rib anomalies, and calcification of the falx cerebri. The challenge in
Priyanka Chhadva, Pete Setabutr
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1998
The basal cell nevus syndrome (BCNS) (nevoid basal-cell carcinoma syndrome, Gorlin syndrome, McKusick MIM 109400) is a rare, multisystem, heritable disorder. Evidence exists for its presence in Egyptian mummies, and cases were described initially a century ago.
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The basal cell nevus syndrome (BCNS) (nevoid basal-cell carcinoma syndrome, Gorlin syndrome, McKusick MIM 109400) is a rare, multisystem, heritable disorder. Evidence exists for its presence in Egyptian mummies, and cases were described initially a century ago.
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Minerva medica, 1986
Six cases of familial basal cell nevus syndrome encountered over the past 20 years are described. The syndrome is fairly rare and its importance derives from the fact that it is associated with skin lesions of the basal cell epithelioma type that are often highly invasive as well as dysontogenic lesions affecting many organs and systems (mandibular ...
A, Andreani, W, Prato, L, Vittone
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Six cases of familial basal cell nevus syndrome encountered over the past 20 years are described. The syndrome is fairly rare and its importance derives from the fact that it is associated with skin lesions of the basal cell epithelioma type that are often highly invasive as well as dysontogenic lesions affecting many organs and systems (mandibular ...
A, Andreani, W, Prato, L, Vittone
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Dermatologica, 1985
A 90-year-old female presented with multiple nevoid basal cell epitheliomas, skeletal defects and jaw cysts. The syndrome is briefly revisited.
J L, Dereume, R, de Sélys, S, Bataille
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A 90-year-old female presented with multiple nevoid basal cell epitheliomas, skeletal defects and jaw cysts. The syndrome is briefly revisited.
J L, Dereume, R, de Sélys, S, Bataille
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2019
The basal cell naevus syndrome, classically described as a triad of multiple basal cell carcinomas, odontogenic keratocysts of the jaws and skeletal anomalies, is well known by oral and plastic surgeons and dermatologists. This paper describes the clinical features in a series of 60 patients, and highlights some problems of diagnosis and management.
Julia A. Woolgar, J. W. Rippin
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The basal cell naevus syndrome, classically described as a triad of multiple basal cell carcinomas, odontogenic keratocysts of the jaws and skeletal anomalies, is well known by oral and plastic surgeons and dermatologists. This paper describes the clinical features in a series of 60 patients, and highlights some problems of diagnosis and management.
Julia A. Woolgar, J. W. Rippin
openaire +1 more source