Karthiga Kannan S, Sivapatha Sundharam B, Manikandan R
Department of Oral Medicine & Radiology, Sree Mookambika Institute of Dental Sciences, Padanilam, Kulasekharam.
Indian J Dent Res. 2006 Jan-Mar;17(1):50-3. doi: 10.4103/0970-9290.29891.
Binkley and Johnson first reported this syndrome in 1951. But it was in 1960, Gorlin-Goltz established the association of basal cell epithelioma, jaw cyst and bifid ribs, a combination which is now frequently known as Gorlin-Goltz syndrome as well as Nevoid Basal Cell Carcinoma Syndrome (NBCCS). NBCCS is inherited as an autosomal dominant trait with high penetrance and variable expressivity. NBCCS is characterized by variety of cutaneous, dental, osseous, opthalmic, neurologic and sexual abnormalities. One such case of Gorlin-Goltz syndrome is reported here with good illustrations.
宾克利和约翰逊于1951年首次报道了这种综合征。但直到1960年,戈林-戈尔茨才确定了基底细胞上皮瘤、颌骨囊肿和肋骨分叉之间的关联,这种组合现在通常被称为戈林-戈尔茨综合征以及痣样基底细胞癌综合征(NBCCS)。NBCCS以常染色体显性特征遗传,具有高外显率和可变表达性。NBCCS的特征是出现各种皮肤、牙齿、骨骼、眼科、神经和性方面的异常。本文报告了一例戈林-戈尔茨综合征病例,并配有清晰的插图。