| Literature DB >> 18203194 |
Isabelle Pénisson-Besnier1, Thibaud Lebouvier, Marie-Pierre Moizard, Marc Ferré, Magalie Barth, Guillaume Marc, Martine Raynaud, Dominique Bonneau.
Abstract
We report on the case of a 44-year-old man affected with the Simpson-Golabi-Behmel syndrome (SGBS) (OMIM 312870) presenting with ischemic stroke due to a dissection of the right internal carotid. Molecular genetic analysis revealed the p.Gly556Arg mutation in exon 8 of the gene encoding glypican 3 (GPC3). This is the second case of a GPC3 missense mutation to be reported. The only risk factor found in this patient was carotid redundancy, a deformation that is significantly associated with spontaneous carotid dissection. The natural history of SGBS in adults is poorly known, and this case raises the question of a possible vascular risk associated with the disease.Entities:
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Year: 2008 PMID: 18203194 DOI: 10.1002/ajmg.a.32154
Source DB: PubMed Journal: Am J Med Genet A ISSN: 1552-4825 Impact factor: 2.802