637 Apical hypertrophic cardiomyopathy — A frequently unrecognized entity in patients with anginal chest pain

1999 ◽  
Vol 1 ◽  
pp. S107-S107
Author(s):  
B SCHNEIDER ◽  
P VILLENA ◽  
E BAHLMANN ◽  
K KUCK
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.


2014 ◽  
Vol 63 (12) ◽  
pp. A844
Author(s):  
Edward James Stephenson ◽  
Danielle Longchamp ◽  
James Malcolmson ◽  
Redha Boubertakh ◽  
Howell Williams ◽  
...  

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 ◽  
...  

2019 ◽  
Vol 13 (1) ◽  
pp. 71-78
Author(s):  
E.Z. Golukhova ◽  
T.V. Mashina ◽  
D.V. Mrikaev ◽  
E.V. Ruzina ◽  
V.S. Grigor’ev ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document