Congenitally Corrected Transposition of the Great Arteries with Severely Stenotic Bicuspid Aortic Valve in an Adult: A Case Report

2011 ◽  
Vol 29 (1) ◽  
pp. E13-E15 ◽  
Author(s):  
Paolo Giuseppe Pino ◽  
Amedeo Pergolini ◽  
Giordano Zampi ◽  
Angela Calicchia ◽  
Claudia Chialastri ◽  
...  
Author(s):  
Zahra Khajali ◽  
Majid Maleki ◽  
Bahram Mohebbi ◽  
Maryam Aliramezany

Congenitally corrected transposition of the great arteries (cc-TGA) is a rare congenital abnormality that occurs in 1 per 33000 live births. This abnormality comprises nearly 0.05% of all congenital heart defects, with at least 90% of cc-TGA patients having associated cardiac defects; some of these associated defects are, however, very rare. In this case report, we describe a 22-year-old man who referred to our hospital for the evaluation of hypertension and cardiac murmurs. Via echocardiography and catheterization, the patient was finally diagnosed with cc-TGA, bicuspid aortic valve, and coarctation of the aorta. He underwent successful percutaneous transarterial coarctoplasty without any complications at early and 6 months’ follow-up visits.


2017 ◽  
Vol 33 (2) ◽  
pp. 155-158 ◽  
Author(s):  
Hrishikesh Sukhadeo Parashi ◽  
Manoj Murlidhar Joshi ◽  
Manish Ramdhan Jadhao ◽  
Kunal Hemant Rawekar ◽  
Krishnarao Narayan Bhosle

2017 ◽  
Vol 20 (2) ◽  
pp. 162-164
Author(s):  
Muhammet Bozgüney ◽  
Burak Açıkgöz ◽  
Hüseyin Ede ◽  
Yunus Keser Yılmaz ◽  
Çiğdem Ünal Kantekin

2014 ◽  
Vol 25 (4) ◽  
pp. e1-e3
Author(s):  
Fotios A. Mitropoulos ◽  
Meletios A. Kanakis ◽  
Constantinos Contrafouris ◽  
Cleo Laskari ◽  
Spyridon Rammos ◽  
...  

2013 ◽  
Vol 24 (5) ◽  
pp. 955-957
Author(s):  
Rajiv Garg ◽  
Bhavesh Thakkar ◽  
Nilesh Oswal

AbstractThe neuro-cutaneous syndrome tuberous sclerosis is commonly associated with rhabdomyomas in various organs including the heart. We are reporting a rare case of a 7-month old male child with congenitally corrected transposition of the great arteries associated with tuberous sclerosis and cardiac rhabdomyomas. To our knowledge, this rare association has not been reported so far.


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