HYPERTROPHIC CARDIOMYOPATHY WITH PARTIAL ANOMALOUS PULMONARY VENOUS CONNECTION AND ATRIAL SEPTAL DEFECT: A RARE PRESENTATION
2017 ◽
Vol 10
(8)
◽
pp. 5
Keyword(s):
Hypertrophic cardiomyopathy (HOCM) is characterized by heterogeneous clinical expression, unique pathophysiology, and diverse natural history.Coexistence of arterial septal defect and partial anomalous pulmonary venous connection (PAPVC) is very rare. Since HOCM is a congenital defect,coexistence of other congenital defects should be kept in mind when we treat the patients. Only very few cases of HOCM with coexisting congenitalanomalies have been reported so far in medical literature. Hence, we report a case of HOCM with atrial septal defect and PAPVC in a 49-year-old malepatient.
1980 ◽
Vol 79
(5)
◽
pp. 776-781
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Keyword(s):
2019 ◽
Vol 73
(15)
◽
pp. S280
2006 ◽
Vol 81
(1)
◽
pp. 224-230
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Keyword(s):
Keyword(s):
2016 ◽
Vol 32
(11)
◽
pp. 1315.e11-1315.e18
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Keyword(s):