Loeys-Dietz syndrome with a novel in-frame SMAD3 deletion diagnosed as a result of postpartum aortic dissection: A case report

Objective: Loeys-Dietz syndrome (LDS) is a rare, autosomal dominant connective tissue disorder which can aggressively affect the aortic vasculature. Limited information is available regarding its impact on pregnancy and postpartum outcomes. Case report: A pregnant 38-year-old nulliparous woman with...

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Κύριοι συγγραφείς:	Takeshi Nagao, Momoko Inoue, Yuki Ito, Takashi Kunihara, Hiroshi Kawame, Osamu Samura, Aikou Okamoto
Μορφή:	Artigo
Γλώσσα:	Inglês
Έκδοση:	Elsevier 2024-03-01
Σειρά:	Taiwanese Journal of Obstetrics & Gynecology
Θέματα:	Aortic dissection Loeys-Dietz syndrome Pregnancy SMAD3 Vertebral artery tortuosity
Διαθέσιμο Online:	http://www.sciencedirect.com/science/article/pii/S1028455924000354
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