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Imaging of Gorlin-Goltz syndrome: Series of 2 cases.
J Oral Maxillofac Pathol
August 2021
Department of Radiodiagnosis, Government Medical College, Srinagar, Jammu and Kashmir, India.
Gorlin-Goltz syndrome (GGS) is a rare autosomal dominant disorder with multisystemic involvement. It is characterized by the triad of multiple baso-cellular epitheliomas, odontogenic keratocysts (OKC) in the jaws and skeletal anomalies. Later, it was found that calcification of falx is also highly specific.
View Article and Find Full Text PDF[Multiple, histologically varied malignancies in a case of Xeroderma pigmentosum with prolonged evolution by surgical interventions].
Rev Chir Oncol Radiol O R L Oftalmol Stomatol Ser Stomatol
April 1991
On the occasion of a case of Xeroderma pigmentosum followed for a period of 12 years the major data concerning this rare affection are presented. This is an autosomal genodermatosis characterized by hypersensitivity of the skin to certain ranges of the UV light spectrum, and the development of lesions especially on the face. The treatment is essentially preventive and consists in avoiding exposure to UV radiation, and also palliative, consisting in medical therapy, physiotherapy and surgery.
View Article and Find Full Text PDF[Multiple epithelioma of pagetoid type in 2 sisters (baso-cellular nevomatosis?)].
Bull Soc Fr Dermatol Syphiligr
October 1970
[MULTIPLE BASO-CELLULAR NEVUS. NEVOID SYNDROME WITH BASO-CELLULAR PREDOMINANCE].
Bull Soc Fr Dermatol Syphiligr
December 1996
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