Unusual Cortical Bone Features in a Patient with Gorlin-Goltz Syndrome: A Case Report
نویسندگان
چکیده
منابع مشابه
unusual cortical bone features in a patient with gorlin-goltz syndrome: a case report
gorlin-goltz syndrome (ggs) consists of ectodermal and mesodermal abnormalities. in this case report we will investigate lower extremity lesions of ggs. a 52-year-old man with ggs underwent skull and lower extremity computer tomography. radiographic findings included cervical spondylosis, transparent areas with slurred margins, and cerebral falx calcification. tibial and fibular specific cortic...
متن کاملUnusual Cortical Bone Features in a Patient with Gorlin-Goltz Syndrome: A Case Report
Gorlin-Goltz syndrome (GGS) consists of ectodermal and mesodermal abnormalities. In this case report we will investigate lower extremity lesions of GGS. A 52-year-old man with GGS underwent skull and lower extremity computer tomography. Radiographic findings included cervical spondylosis, transparent areas with slurred margins, and cerebral falx calcification. Tibial and fibular specific cortic...
متن کاملGorlin-Goltz syndrome – A case Report
Gorlin-Goltz syndrome is a rare autosomal dominant disorder that involves multiple organ systems, including the skin, skeleton and jaws. We report a case of young female with multiple odontogenic keratocysts, high arched palate, euryopia, palmer pits, solitary, pigmented nevus , areas of hyper-pigmentation in the upper eyelid of left eye, dorsal surface of hands, calcified diaphragma sellae, ri...
متن کامل[Gorlin-Goltz syndrome--a case report].
UNLABELLED The Gorlin-Goltz syndrome (GGS) (the nevoid basal cell carcinoma syndrome-NBCCS) is an autosomal dominant syndrome caused by mutations found on chromosome 9. The syndrome is characterized by increased predisposition to develop a basal cell carcinoma and associated with multiorgan anomalies. THE AIM OF THIS WORK To present a case of GGS and explain modern standards of care for patie...
متن کاملGorlin-Goltz syndrome: A rare case report
Gorlin-Goltz syndrome (GS), also known as nevoid basal cell carcinoma syndrome, is an infrequent multisystem disease inherited in a dominant autosomal way, which shows a high level of penetrance and variable expressiveness. It is characterised by keratocystic odontogenic tumours (KCOT) in the jaw, multiple basal cell nevi carcinomas and skeletal abnormalities. This syndrome may be diagnosed ear...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: Iranian Journal of Radiology
سال: 2014
ISSN: 1735-1065,2008-2711
DOI: 10.5812/iranjradiol.5316