Rao, Karthik N and Patil, Navin and Balaji, O and Kotian, Rahul P (2017) Hypertrophic cardiomyopathy with partial anomalous pulmonary venous connection and atrial septal defect: A rare presentation. Asian Journal of Pharmaceutical and Clinical Research, 10 (8). pp. 5-7. ISSN 0974-2441
![]() |
PDF
00003288.pdf - Published Version Restricted to Registered users only Download (481kB) | Request a copy |
Abstract
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 congenital anomalies 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 male patient.
Item Type: | Article |
---|---|
Uncontrolled Keywords: | Hypertrophic cardiac myopathy; Atrial septal defect; Coronary artery disease; Anomalous pulmonary venous connection. |
Subjects: | Allied Health > MCOAHS Manipal > Medical Imaging Tech Medicine > KMC Manipal > Medicine Medicine > KMC Manipal > Pharmacology |
Depositing User: | KMC Library |
Date Deposited: | 16 Oct 2017 05:02 |
Last Modified: | 16 Oct 2017 05:02 |
URI: | http://eprints.manipal.edu/id/eprint/149823 |
Actions (login required)
![]() |
View Item |