( I – 2A.0 ; IV – 1D.2d ) Przypadek 43 letniego mężczyzny z tętniakowatym poszerzeniem aorty wstępującej oraz po implantacji sztucznej zastawki aortalnej Natalia Dłużniewska MD; Lidia Tomkiewicz – Pająk MD, PhD; Aleksandra Lenart MD, Monika Smaś – Suska MD, Prof. Maria Olszowska MD, PhD; Prof. Piotr Podolec MD, PhD
EKSPERTYZA 1 “Development of the European Network in Orphan Cardiovascular Diseases” “Rozszerzenie Europejskiej Sieci Współpracy ds. Sierocych Chorób Kardiologicznych”
Posted in 1. Abnormalities of the position and connection of the heart and vessels, 2. Connective tissue disorders causing aneurysmal disease, 2. Left heart valves, A. Aneurysmal disease of the aorta, Przypadki kliniczne, D. Valves, I. Rare diseases of systemic circulation, IV. Rare congenital cardiovascular diseases, Others
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(I-2A.1) (English) 54-year-old female with Marfan’s Syndrome Prof. Podolec P. MD, PhD, Kopeć G.MD, PhD, Rubiś P. MD, PhD, Dziedzic-Oleksy H. MD, Hlawaty M. MD, PhD
Keywords: Marfan’s Syndrome, aortic dissection Background Marfan’s Syndrome is an inherited autosomal dominant disorder of connective tissue, that affects many organs including the cardiovascular, ocular, skeletal and pulmonary system, the skin and the dura. The classical cardiovascular manifestations of Marfan’s Syndrome are mitral valve prolapse and aortic root dilation, leading to aneurysm and dissection. Regular control studies such as echocardiography, magnetic resonance and computed tomography are required in patients with this disease. Case description A 54-year-old Caucasian female with Marfan’s …