Gorlin R J, Sedano H O
Birth Defects Orig Artic Ser. 1971 Jun;7(8):140-8.
Over a decade has elapsed since the senior author became interested in the multiple nevoid basal cell carcinoma syndrome. During the intervening years many facets of the syndrome have been examined and the evidence weighed concerning new findings. The original triad of signs, multiple nevoid basal cell carcinomas, jaw cysts and skeletal anomalies, has been greatly expanded to include intracranial calcification, ovarian fibroma, lymphomesenteric cysts, medulloblastoma and a whole host of minor and occasional (but valid) associated anomalies.
自从资深作者对多发性痣样基底细胞癌综合征产生兴趣以来，已经过去了十多年。在这期间，该综合征的许多方面都得到了研究，并对新发现的证据进行了权衡。最初的三联征，即多发性痣样基底细胞癌、颌骨囊肿和骨骼异常，已经大大扩展，包括颅内钙化、卵巢纤维瘤、肠系膜囊肿、髓母细胞瘤以及许多轻微和偶发（但确实存在）的相关异常。
