aortic arch syndrome
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2017 ◽  
Vol 35 (2) ◽  
pp. 91-96
Author(s):  
SM Shaheedul Islam ◽  
Sahela Nasrin ◽  
F Aaysha Cader ◽  
M Maksumul Haq ◽  
Syed Dawood Md Taimur

Takayasu arteritis (TA) is a chronic granulomatous vasculitic disease of the aorta and its major branches, predominantly affecting young females of Asian origin. Also known as Aortic arch syndrome, the condition has been better documented as the ‘Pulse less disease’ leading to claudication, bruits, absent or reduced brachial or radial pulses and aortic incompetence. However, a ‘prepulseless’ stage of TA exists, characterized by non-specific constitutional symptoms, hypertension and raised inflammatory markers. We report the case of an 18- year-old Bangladeshi female presenting with hypertension, moderate to severe aortic regurgitation (AR) and fever, diagnosed and treated as a case of pre-pulseless TA.J Bangladesh Coll Phys Surg 2017; 35(2): 91-96


2014 ◽  
Vol 3 (3) ◽  
pp. 304-305
Author(s):  
Kevser Peker ◽  
Recai Dagli ◽  
Yildiz Babadag

2012 ◽  
Vol 21 (11) ◽  
pp. 745-746 ◽  
Author(s):  
Rajeev L. Narayan ◽  
Anubhav Kanwar ◽  
Adam Jacobi ◽  
Javier Sanz

2008 ◽  
Vol 67 (7) ◽  
pp. 1030-1033 ◽  
Author(s):  
M Both ◽  
K Ahmadi-Simab ◽  
M Reuter ◽  
O Dourvos ◽  
E Fritzer ◽  
...  

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