Article
Exome sequencing in seven families and gene-based association studies indicate genetic heterogeneity and suggest possible candidates for fibromuscular dysplasia.
Journal of hypertension - 1 Sept 2015
Kiando Soto Romuald, Barlassina Cristina, Cusi Daniele, Galan Pilar, Lathrop Mark, Plouin Pierre-François, Jeunemaitre Xavier, Bouatia-Naji Nabila
Abstract excerpt
BACKGROUND: Fibromuscular dysplasia (FMD) is a nonatherosclerotic vascular disease leading to stenosis, aneurysm and dissection, mainly of renal arteries and carotids. FMD occurs predominantly in women with nearly four out of 1000 prevalence and cause hypertension, renal ischemia or stroke. The pathogenesis of FMD is unknown and a genetic origin is suspected given its demonstrated familial aggregation. METHOD: We...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.
