痣样基底细胞癌综合征
生物
修补
基底细胞痣综合征
病理
基底细胞癌
异位钙化
PTCH1型
表型
癌症研究
基因
遗传学
钙化
医学
基底细胞
刺猬信号通路
作者
Abirami Chidambaram,Alisa M. Goldstein,Mae R. Gailani,Bernard Gerrard,Sherri J. Bale,John J. DiGiovanna,A E Bale,Michael Dean
出处
期刊:PubMed
日期:1996-10-15
卷期号:56 (20): 4599-601
被引量:135
摘要
The nevoid basal cell carcinoma syndrome (NBCCS), or Gorlin syndrome, is a multisystem autosomal dominant disorder. The salient features of this syndrome include multiple basal cell carcinomas, palmar and/or plantar pits, odontogenic keratocysts, skeletal and developmental anomalies, and ectopic calcification. Other features include such tumors as ovarian fibromas and medulloblastomas. There is extensive interfamilial as well as intrafamilial variability with respect to the manifestation and severity of the phenotype. Alterations in the human homologue (PTCH) of the Drosophila segment polarity gene patched have been identified in NBCCS patients as well as tumors associated with this syndrome. We report several mutations in this gene in NBCCS patients and present the clinical phenotypes of the individuals in whom these mutations were identified.
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