Clinical and mutation-type analysis from an international series of 198 probands with a pathogenic FBN1 exons 24-32 mutation

L. Faivre, G. Collod-Beroud, B. Callewaert, A. Child, C. Binquet, E. Gautier, B. L. Loeys, E. Arbustini, K. Mayer, M. Arslan-Kirchner, C. Stheneur, A. Kiotsekoglou, P. Comeglio, N. Marziliano, J. E. Wolf, O. Bouchot, P. Khau-Van-Kien, C. Beroud, M. Claustres, C. Bonithon-KoppP. N. Robinson, L. Adès, J. De Backer, P. Coucke, U. Francke, A. De Paepe, G. Jondeau, C. Boileau

Research output: Contribution to journalArticlepeer-review

Abstract

Mutations in the FBN1 gene cause Marfan syndrome (MFS) and a wide range of overlapping phenotypes. The severe end of the spectrum is represented by neonatal MFS, the vast majority of probands carrying a mutation within exons 24-32. We previously showed that a mutation in exons 24-32 is predictive of a severe cardiovascular phenotype even in non-neonatal cases, and that mutations leading to premature truncation codons are under-represented in this region. To describe patients carrying a mutation in this so-called 'neonatal' region, we studied the clinical and molecular characteristics of 198 probands with a mutation in exons 24-32 from a series of 1013 probands with a FBN1 mutation (20%). When comparing patients with mutations leading to a premature termination codon (PTC) within exons 24-32 to patients with an in-frame mutation within the same region, a significantly higher probability of developing ectopia lentis and mitral insufficiency were found in the second group. Patients with a PTC within exons 24-32 rarely displayed a neonatal or severe MFS presentation. We also found a higher probability of neonatal presentations associated with exon 25 mutations, as well as a higher probability of cardiovascular manifestations. A high phenotypic heterogeneity could be described for recurrent mutations, ranging from neonatal to classical MFS phenotype. In conclusion, even if the exons 24-32 location appears as a major cause of the severity of the phenotype in patients with a mutation in this region, other factors such as the type of mutation or modifier genes might also be relevant.

Original languageEnglish
Pages (from-to)491-501
Number of pages11
JournalEuropean Journal of Human Genetics
Volume17
Issue number4
DOIs
Publication statusPublished - 2009

ASJC Scopus subject areas

  • Genetics(clinical)
  • Genetics

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