Results 131 to 140 of about 5,083 (170)
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The Journal of Laryngology & Otology, 1975
The uncommon familial syndrome of multiple odontogenic keratocysts, basal cell naevi and skeletal anomalies is reviewed, and seven cases are described, including one patient who developed squamous cell carcinoma in a previous odontogenic keratocyst of the maxilla.
R T, Ramsden, A, Barrett
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The uncommon familial syndrome of multiple odontogenic keratocysts, basal cell naevi and skeletal anomalies is reviewed, and seven cases are described, including one patient who developed squamous cell carcinoma in a previous odontogenic keratocyst of the maxilla.
R T, Ramsden, A, Barrett
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Gorlin's syndrome and the heart
British Journal of Oral Surgery, 1979Three further cases of the Multiple Basal Cell Naevi Syndrome are added to the literature. One case developed a neonatal left ventricular fibroma, subsequently successfully excised. An association between the syndrome and cardiac tumours has not been documented before, and the relative frequencies of the two conditions are discussed.
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2005
Abstract Gorlin syndrome, which is also widely known as basal cell naevus syndrome (BCNS) or nevoid basal cell carcinoma syndrome (NBCCS), was first fully delineated in 1960 (1). It is an autosomal dominant condition with high penetrance, although occasional patients may not have clear features on clinical assessment, even in adult life (
Helen V. Firth +2 more
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Abstract Gorlin syndrome, which is also widely known as basal cell naevus syndrome (BCNS) or nevoid basal cell carcinoma syndrome (NBCCS), was first fully delineated in 1960 (1). It is an autosomal dominant condition with high penetrance, although occasional patients may not have clear features on clinical assessment, even in adult life (
Helen V. Firth +2 more
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Acta dermatovenerologica Alpina, Pannonica, et Adriatica, 2007
Gorlin-Goltz syndrome, also known as basal cell nevus syndrome, is an uncommon, autosomal dominant inherited disorder, which is characterized by numerous basal cell carcinomas, maxillary keratocysts, and musculoskeletal malformations. Occasionally, it is associated with aggressive basal cell carcinomas and internal malignancies.
Binić, Ivana +4 more
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Gorlin-Goltz syndrome, also known as basal cell nevus syndrome, is an uncommon, autosomal dominant inherited disorder, which is characterized by numerous basal cell carcinomas, maxillary keratocysts, and musculoskeletal malformations. Occasionally, it is associated with aggressive basal cell carcinomas and internal malignancies.
Binić, Ivana +4 more
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Location of gene for Gorlin syndrome
The Lancet, 1992The Gorlin (naevoid-basal-cell-carcinoma) syndrome is an autosomal dominant disorder characterised by multiple naevoid basal-cell carcinomas, recurrent odontogenic keratocysts, skeletal anomalies, intracranial calcification, and developmental malformations.
Farndon, P. A. +3 more
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Acta medica portuguesa, 1997
The major features of the nevoid basal-cell carcinoma syndrome are epidermal multiple cell carcinomas, cysts of the jaws and skeletal abnormalities, mainly in the ribs. The authors have reviewed the literature concerning multiple anomalies which are associated to this syndrome, and report a clinical case, emphasizing the advantages of early diagnosis ...
B, do Amaral +2 more
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The major features of the nevoid basal-cell carcinoma syndrome are epidermal multiple cell carcinomas, cysts of the jaws and skeletal abnormalities, mainly in the ribs. The authors have reviewed the literature concerning multiple anomalies which are associated to this syndrome, and report a clinical case, emphasizing the advantages of early diagnosis ...
B, do Amaral +2 more
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Gorlin's syndrome with ameloblastoma
Oral Surgery, Oral Medicine, Oral Pathology, 1978M F, Jensen, S M, Roser
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2000
Gorlin syndrome is a hereditary disease characterized by congenital anomalies of skin and of the skeletal, reproductive, and central nervous systems. Two patients, a 19-year-old man and a 27-year-old woman, are described. Both patients complained of multiple pigmentary lesions on the face and the trunk that had been present since childhood and ...
CALTABIANO, ROSARIO +3 more
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Gorlin syndrome is a hereditary disease characterized by congenital anomalies of skin and of the skeletal, reproductive, and central nervous systems. Two patients, a 19-year-old man and a 27-year-old woman, are described. Both patients complained of multiple pigmentary lesions on the face and the trunk that had been present since childhood and ...
CALTABIANO, ROSARIO +3 more
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Gorlin Syndrome: Recent Advances in Genetic Testing and Molecular and Cellular Biological Research
International Journal of Molecular Sciences, 2020Shoko Onodera
exaly