| Literature DB >> 19059503 |
F S Van Dijk1, B C Hamel, Y Hilhorst-Hofstee, B J M Mulder, J Timmermans, G Pals, J M Cobben.
Abstract
We report two families in which the probands have compound-heterozygous Marfan syndrome (MFS). The proband of family 1 has the R2726W FBN1 mutation associated with isolated skeletal features on one allele and a pathogenic FBN1 mutation on the other allele. The phenotype of the compound-heterozygous probands appears to be more severe than that of their heterozygous family members which underlines the possibility that certain trans-located FBN1 mutations might act as modifiers of phenotype explaining some of the intrafamilial variability in Marfan syndrome.Entities:
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Year: 2008 PMID: 19059503 DOI: 10.1016/j.ejmg.2008.11.004
Source DB: PubMed Journal: Eur J Med Genet ISSN: 1769-7212 Impact factor: 2.708