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

• Asıl Yazarlar: Takeshi Nagao (Yazar), Momoko Inoue (Yazar), Yuki Ito (Yazar), Takashi Kunihara (Yazar), Hiroshi Kawame (Yazar), Osamu Samura (Yazar), Aikou Okamoto (Yazar)
• Materyal Türü: Kitap
• Baskı/Yayın Bilgisi: Elsevier, 2024-03-01T00:00:00Z.
• Konular: article
• Online Erişim: Connect to this object online.

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...