The role of connective tissue genomics in ascending aortic dissection: A case of Marfan syndrome

AuthorFiroozeh Madadien
Authormanouchehr hekmaten
AuthorZahra Ansari Avalen
AuthorAbdolhamid Bagherien
AuthorKamal Fanien
AuthorMohammad Hosein Ghanbarpouren
Authormaryam hamidzaden
AuthorMehrubon Murodoven
AuthorAli Dabbaghen
OrcidFiroozeh Madadi [0000-0001-9293-1440]en
OrcidZahra Ansari Aval [0000-0001-5019-2563]en
OrcidKamal Fani [0000-0002-7921-257X]en
OrcidAli Dabbagh [0000-0003-4344-8131]en
Issued Date2019-09-30en
AbstractBackground: Aortic dissection is a rare yet life threating condition with some already discovered risk factors namely hypertension, connective tissue disorders such as Marfan syndrome (MFS), cocaine abuse and cigarette smoking.Case report: In this article we would like to present a case of MFS who presented with severe chest pain and undergone Bentall surgery due to aortic dissection and aneurysm.Conclusion: Although many risk factors and preventive measures are already investigated, there is no definite method to avoid its occurrence in genetically predisposed patients such as MFS. Patient-specific models utilizing embryonic stem cells (ESC) and induced pluripotent stem cells (iPSC) may offer some advantages.en
DOIhttps://doi.org/10.22037/jcma.v4i3.28189en
URIhttps://brieflands.com/journals/jcma/articles/149588en
KeywordMarfan syndrome - Aortic dissection - iPSC - cocaineen
PublisherBrieflandsen
TitleThe role of connective tissue genomics in ascending aortic dissection: A case of Marfan syndromeen
TypeBrief Reporten

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