Results 51 to 60 of about 21,536 (218)

Etiology and distribution of isolated aortic stenosis in Indian patients – A study from a large tertiary care hospital in north India

Indian Heart Journal, 2020
Background: Isolated aortic valve disease (IAVD) has traditionally been a disease of elderly, etiology being either senile degeneration of a tricuspid aortic valve or calcification of a bicuspid aortic valve.
Ankit Kumar Sahu, Pramod Sagar, Roopali Khanna, Sudeep Kumar, Satyendra Tewari, Aditya Kapoor, Naveen Garg, Pravin K. Goel   +7 more
doaj   +1 more source

Heartbeat: phenotypic heterogeneity of bicuspid aortic valve disease [PDF]

Heart, 2018
Bicuspid aortic valve (BAV) disease is common, affecting 1%–2% of the entire population, with nearly all BAV patients eventually requiring aortic valve replacement, often with concurrent aortic surgery for dilation of the sinuses or ascending aorta. Although echocardiography allows easy diagnosis of the presence of BAV disease early in life, we are ...
openaire   +2 more sources

Three Stage Hybrid Approach for Congenital Aortic Coarctation and Bicuspid Aortic Valve With Severe Aortic Stenosis in an Adult Patient

EJVES Short Reports, 2019
Introduction: Untreated congenital aortic coarctation and valvular abnormalities are rare in an adult patient and require complex management. Report: A 68 year old woman with congenital aortic coarctation and bicuspid aortic valve with severe aortic ...
Monica M. Matsumoto, Ross Milner
doaj   +1 more source

Cerebrovascular complications and infective endocarditis. impact of available evidence on clinical outcome [PDF]

, 2018
Infective endocarditis (IE) is a life-threatening disease. Its epidemiological profile has substantially changed in recent years although 1-year mortality is still high.
De Bellis, Antonio, D’Abramo, Mizar, Frati, Giacomo, Greco, Ernesto, Iaccarino, Alessandra, Mestres, Carlos-A., Saade, Wael, Schirone, Leonardo, Sciarretta, Sebastiano   +8 more
core   +1 more source

Evolving treatment options for valve and aortic disease with bicuspid aortic valve [PDF]

Annals of Translational Medicine, 2017
Treatment decisions for patients with bicuspid aortic valves (BAVs) are unique for two principal reasons: (I) aortopathy with dilation of the proximal aorta is seen about 50% of cases, and frequently requires a combined repair; (II) patients are significantly younger than those undergoing treatment for acquired aortic valve disease, making the ...
Nicholas S, Burris, Michael D, Hope
openaire   +2 more sources

Dissection of the aorta, a rare combination of coarctation, a bicuspid aortic valve, and hypertension in a young patient

The Egyptian Journal of Internal Medicine, 2012
Aortic dissection is an uncommon but very lethal disease. Majority of cases are found in elderly patients with a history of hypertension. Young patients usually have other risk factors such as vasculitis, Marfan syndrome, unrecognized coarctation of the ...
Abdulrahman Aldousari, Amir Masud, Mohsin Mahmood   +2 more
doaj   +1 more source

Transcatheter treatment of complex pulmonic and aortic valvular disease following failed Ross procedure

Clinical Case Reports, 2021
A 63‐year‐old man with congenital bicuspid aortic valve disease and complex surgical history (that includes a Ross procedure complicated by cardiac arrest requiring emergency coronary artery bypass graft surgery, multiple subsequent sternotomies to treat
Mohammad Aziz, Rajbir Sidhu, Curtiss T. Stinis   +2 more
doaj   +1 more source

Bicuspid aortic valve disease: systematic review and meta-analysis of surgical aortic valve repair [PDF]

, 2016
Objective: Aortic valve repair is still emerging and its role in the treatment of bicuspid aortic valve disease (BAVD) is not yet fully understood.

core   +1 more source

Differentiating the Clinical and Variant Spectrum of Hardikar Syndrome From Other MED12‐Related Developmental Disorders

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT The rare X‐linked female‐restricted Hardikar syndrome (HDKR, OMIM # 301068) is characterized by multiple congenital anomalies including orofacial clefts, gastrointestinal, genitourinary, and cardiac anomalies, but cognitive and neurobehavioral development is rarely impaired.
Tinne Warmoeskerken, Miel Theunis, Kris Van den Bogaert, Koenraad Devriendt, Jeroen Breckpot   +4 more
wiley   +1 more source

Candidate gene resequencing in a large bicuspid aortic valve-associated thoracic aortic aneurysm cohort: SMAD6 as an important contributor [PDF]

, 2017
Bicuspid aortic valve (BAV) is the most common congenital heart defect. Although many BAV patients remain asymptomatic, at least 20% develop thoracic aortic aneurysm (TAA).
Alaerts, M. (Maaike), Albuisson, J. (Juliette), Andelfinger, G. (Gregor), Beek, G. (Gerarda van de), Björck, H.M. (Hanna M.), Bolar, N. (Nikhita), Cannaerts, E. (Elyssa), Dietz, H.C. (Harry ), Duijnhouwer, T. (Toon), Eriksson, P. (Per), Franco-Cereceda, A. (Anders), Gillis, E. (Elisabeth), Goudot, G. (Guillaume), Gould, R.A. (Russell A.), Jeunemaître, X. (Xavier), Kempers, M.J.E. (Marlies), Krebsova, A. (Alice), Kumar, A.A. (Ajay A.), Laar, I.M.B.H. (Ingrid) van de, Laer, L. (Lut) van, Loeys, B.L. (Bart), Luyckx, I. (Ilse), McCallion, A.S. (Andrew), Meester, J. (Josephina), Mertens, L. (Luc), Messas, E. (Emmanuel), Mital, S. (Seema), Mohamed, S.A. (Salah A.), Nemcikova, M. (Michaela), Preuss, C. (Christoph), Salemink, S. (Simone), Vandeweyer, G. (Geert), Verhagen, J.M.A. (Judith), Verstraeten, A. (Aline), Wessels, M.W. (Marja), Wieschendorf, B. (Björn), Wünnemann, F. (Florian), Zerbino, D. (Dmytro), Zhurayev, R. (Rustam)   +38 more
core   +6 more sources