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- W2066142439 abstract "Gorlin's syndrome (also known as basal cell nevus syndrome, Gorlin-Goltz syndrome, and nevoid basal cell carcinoma syndrome) is a rare, inherited disorder characterized by multiple basal-cell epitheliomas, intracranial calcification, keratocysts of the mandible, and unusual and striking skeletal abnormalities. We present the interesting case of a 45-year-old woman who was informed that she had fibrous dysplasia of the extremity at another institution before extensive radiological work-up showed a diffuse skeletal process. The skeletal abnormalities, in conjunction with the patient's history of multiple basal cell carcinomas, is consistent with the diagnosis of Gorlin's syndrome. We describe this unusual case of striking radiological and scintigraphic findings in a patient with Gorlin's syndrome." @default.
- W2066142439 created "2016-06-24" @default.
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- W2066142439 date "2003-08-11" @default.
- W2066142439 modified "2023-09-27" @default.
- W2066142439 title "Gorlin's syndrome: Diffuse appendicular skeletal involvement with scintigraphic correlation" @default.
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- W2066142439 doi "https://doi.org/10.1046/j.1440-1673.2003.01186.x" @default.
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