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Isolated aneurysmal disease as an underestimated finding in individuals with JAG1 pathogenic variants.

Jotte Rodrigues BentoAlice KrebsováIlse Van GuchtIrene Valdivia CallejonAn Van BerendoncksPavel VotypkaIlse LuyckxPetra PeldovaSteven LagaMarek HavelkaLut Van LaerPavel TruneckaNele BoeckxAline VerstraetenMilan MacekJosephina A N MeesterBart L Loeys
Published in: Human mutation (2022)
Pathogenic variants in JAG1 are known to cause Alagille syndrome (ALGS), a disorder that primarily affects the liver, lung, kidney, and skeleton. Whereas cardiac symptoms are also frequently observed in ALGS, thoracic aortic aneurysms have only been reported sporadically in postmortem autopsies. We here report two families with segregating JAG1 variants that present with isolated aneurysmal disease, as well as the first histological evaluation of aortic aneurysm tissue of a JAG1 variant carrier. Our observations shed more light on the pathomechanisms behind aneurysm formation in JAG1 variant harboring individuals and underline the importance of cardiovascular imaging in the clinical follow-up of such individuals.
Keyphrases
  • copy number
  • aortic aneurysm
  • left ventricular
  • coronary artery
  • high resolution
  • spinal cord
  • pulmonary artery
  • gene expression
  • pulmonary hypertension
  • physical activity
  • genome wide
  • depressive symptoms
  • aortic dissection