scholarly journals APICAL HYPERTROPHIC CARDIOMYOPATHY: CHEST PAIN AND PERFUSION DEFECTS ARE ASSOCIATED WITH CAVITY OBLITERATION AND POST-SYSTOLIC STRAIN

2014 ◽  
Vol 63 (12) ◽  
pp. A844
Author(s):  
Edward James Stephenson ◽  
Danielle Longchamp ◽  
James Malcolmson ◽  
Redha Boubertakh ◽  
Howell Williams ◽  
...  
2019 ◽  
Vol 29 (12) ◽  
pp. 1533-1535 ◽  
Author(s):  
Qu-ming Zhao ◽  
Lan He ◽  
Fang Liu

AbstractApical hypertrophic cardiomyopathy is an uncommon morphologic variant of hypertrophic cardiomyopathy, which is rarely diagnosed in childhood. To date, very few cases of asymptomatic children younger than 18 years have been reported in the literature. To the best of our knowledge, this is the first case of paediatric apical hypertrophic cardiomyopathy presenting with exertional chest pain, with characteristic electrocardiographic, echocardiographic, MRI, and cardiac angiography findings.


Heart ◽  
2016 ◽  
Vol 102 (15) ◽  
pp. 1215-1220 ◽  
Author(s):  
Hyungseop Kim ◽  
Jung-Ho Park ◽  
Ki-Bum Won ◽  
Hyuck-Jun Yoon ◽  
Hyoung-Seob Park ◽  
...  

2003 ◽  
Vol 42 (2) ◽  
pp. 288-295 ◽  
Author(s):  
Kinya Matsubara ◽  
Takashi Nakamura ◽  
Toshiro Kuribayashi ◽  
Akihiro Azuma ◽  
Masao Nakagawa

Author(s):  
Hatim Al Lawati ◽  
Marwa Al Habsi ◽  
Adil B Al Riyami

Abstract Apical Hypertrophic Cardiomyopathy (Ap-HCM) also known as Yamaguchi Disease is characterized by limited involvement of the left ventricular (LV) apex. It can present with typical ischaemic chest pain, dyspnoea and arrhythmias. We report the case of patient with ischaemic chest pain who was diagnosed with Ap-HCM at the time of coronary angiography. We share representative images from his cardiac evaluation.


2018 ◽  
Vol 251 ◽  
pp. 65-70 ◽  
Author(s):  
Edward Stephenson ◽  
Pierre Monney ◽  
Francesca Pugliese ◽  
James Malcolmson ◽  
Steffen E. Petersen ◽  
...  

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