| Literature DB >> 30352675 |
Julia Taeubner1, Dagmar Wieczorek2, Layal Yasin1, Triantafyllia Brozou1, Arndt Borkhardt1, Michaela Kuhlen3.
Abstract
Inherited diseases are not always expressed in the same way in every individual that carries the same variant in a disease-causing gene. This phenomenon is known as reduced or incomplete penetrance. Variable and incomplete penetrance may explain why inherited diseases are occasionally transmitted through unaffected parents, but also why clinically healthy individuals can carry potentially pathogenic variants without expressing features of the disease. Here, we will provide an overview of factors that play a fundamental role in the concept of penetrance and expressivity of cancer predisposing genes in children with malignancies. These findings are important to understand the complexity of inherited diseases and cancer development and to improve genetic counselling for the affected families.Entities:
Keywords: cancer predisposition syndrome; children; expressivity; gene penetrance; genetic counselling; modifier genes
Mesh:
Year: 2018 PMID: 30352675 DOI: 10.1016/j.trecan.2018.09.002
Source DB: PubMed Journal: Trends Cancer ISSN: 2405-8025