| Literature DB >> 30006056 |
Saleh Albanyan1, Rachel H Giles2, Enric Mocholi Gimeno3, Josh Silver4, Jillian Murphy4, Hanna Faghfoury5, Chantal F Morel5, Jerry Machado6, Raymond H Kim7.
Abstract
Von Hippel-Lindau (VHL) disease is a hereditary tumor syndrome in which carriers are at an increased risk of developing a variety of tumors in multiple organ systems. A clinical diagnosis of VHL is determined by the presence of specific clinical manifestations while a molecular genetic diagnosis results from a pathogenic variant in the VHL gene. The majority of mutations occur in VHL coding exons and DNA analysis of these regions has a reported sensitivity of nearly 100%. However, rare variants in the VHL gene promoter may be detected in some cases of suspected VHL disease. We report two cases where VHL promoter variants were detected and describe the role of multi-step mRNA and protein analysis in the diagnostic evaluation of these cases.Entities:
Keywords: Promoter; Protein; VHL; mRNA
Mesh:
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Year: 2018 PMID: 30006056 DOI: 10.1016/j.ejmg.2018.07.006
Source DB: PubMed Journal: Eur J Med Genet ISSN: 1769-7212 Impact factor: 2.708