Literature DB >> 18203194

Carotid artery dissection in an adult with the Simpson-Golabi-Behmel syndrome.

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.

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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


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