Lo Muzio L, Nocini P F, Savoia A, Consolo U, Procaccini M, Zelante L, Pannone G, Bucci P, Dolci M, Bambini F, Solda P, Favia G
Division of Oral Pathology and Medicine, University Federico II, Naples, Italy.
Clin Genet. 1999 Jan;55(1):34-40. doi: 10.1034/j.1399-0004.1999.550106.x.
Nevoid basal cell carcinoma syndrome (NBCCS) is a hereditary condition transmitted as an autosomal dominant trait with complete penetrance and variable expressivity. The syndrome is characterised by numerous basal cell carcinomas (BCCs), odontogenic keratocysts of the jaws, palmar and/or plantar pits, skeletal abnormalities and intracranial calcifications. In this paper, the clinical features of 37 Italian patients are reviewed. Jaw cysts and calcification of falx cerebri were the most frequently observed anomalies, followed by BCCs and palmar/plantar pits. Similar to the case of African Americans, the relatively low frequency of BCCs in the Italian population is probably due to protective skin pigmentation. A future search based on mutation screening might establish a possible genotype phenotype correlation in Italian patients.
痣样基底细胞癌综合征(NBCCS)是一种遗传性疾病,以常染色体显性特征遗传,具有完全外显率和可变表达性。该综合征的特征为多发性基底细胞癌(BCC)、颌骨牙源性角化囊肿、手掌和/或足底凹痕、骨骼异常和颅内钙化。本文回顾了37例意大利患者的临床特征。颌骨囊肿和大脑镰钙化是最常观察到的异常,其次是基底细胞癌和手掌/足底凹痕。与非裔美国人的情况类似,意大利人群中基底细胞癌相对较低的发病率可能归因于具有保护作用的皮肤色素沉着。未来基于突变筛查的研究可能会在意大利患者中建立起可能的基因型与表型的相关性。