Results 31 to 40 of about 445,510 (263)

Implications of Genetic Testing in Dilated Cardiomyopathy

Circulation Genomic and Precision Medicine, 2020
Supplemental Digital Content is available in the text. Background: Genetic analysis is a first-tier test in dilated cardiomyopathy (DCM). Electrical phenotypes are common in genetic DCM, but their exact contribution to the clinical course and outcome is ...
J. Verdonschot, M. Hazebroek, I. Krapels, M. Henkens, A. Raafs, Ping Wang, J. Merken, G. Claes, E. Vanhoutte, A. van den Wijngaard, S. Heymans, H. Brunner   +11 more
semanticscholar   +1 more source

Anaesthetic Management of a Patient with Dilated Cardiomyopathy for Fracture Femur Surgery-A Case Report [PDF]

Journal of Clinical and Diagnostic Research, 2014
Dilated cardiomyopathy (DCM) is defined as impairment of the ventricular function of the myocardium. The management of a patient with dilated cardiomyopathy, who undergoes a non-cardiac surgery, is always a challenge for an anaesthesiologist, as this ...
Koramutla Pradeep Kumar, Gudaru Jagadesh
doaj   +1 more source

Dysregulation of Calcium Handling in Duchenne Muscular Dystrophy-Associated Dilated Cardiomyopathy: Mechanisms and Experimental Therapeutic Strategies

Journal of Clinical Medicine, 2020
Duchenne muscular dystrophy (DMD) is an X-linked recessive disease resulting in the loss of dystrophin, a key cytoskeletal protein in the dystrophin-glycoprotein complex.
M. Law, Houda Cohen, Ashley A. Martin, A. B. B. Angulski, J. Metzger   +4 more
semanticscholar   +1 more source

Familial Dilated Cardiomyopathy [PDF]

Heart, Lung and Circulation, 2020
Advances in human genome sequencing have re-invigorated genetics studies of dilated cardiomyopathy (DCM), facilitating genetic testing and clinical applications. With a range of genetic testing options now available, new challenges arise for data interpretation and identifying single pathogenic variants from the many thousands of rare variants present ...
Ray E. Hershberger, Stacey Peters, Samuel Birch, Renee Johnson, Dominica Zentner, Diane Fatkin, Diane Fatkin, Diane Fatkin   +7 more
openaire   +7 more sources

Epigenetics in dilated cardiomyopathy [PDF]

Current Opinion in Cardiology, 2019
Characterized by enlarged ventricle and loss of systolic function, dilated cardiomyopathy (DCM) has the highest morbidity among all the cardiomyopathies. Although it is well established that DCM is typically caused by mutations in a large number of genes, there is an emerging appreciation for the contribution of epigenetic alteration in the development
Yu, Junyi, Zeng, Chunyu, Wang, Yibin
openaire   +4 more sources

Role of Cardiac Magnetic Resonance Imaging in Hypocalcemia-Induced Dilated Cardiomyopathy in Pediatric Population

Indian Journal of Radiology and Imaging, 2021
Background Hypocalcemia is a rare reversible cause of dilated cardiomyopathy in pediatric population. Myocarditis is another more frequent cause of cardiomyopathy with overlapping presenting features.
Ankit Garg, Sushil Azad, Khemendra Kumar, Mona Bhatia, S. Radhakrishnan   +4 more
doaj   +1 more source

Variant Interpretation for Dilated Cardiomyopathy

Circulation Genomic and Precision Medicine, 2020
Supplemental Digital Content is available in the text. Background: The hypothesis of the Dilated Cardiomyopathy Precision Medicine Study is that most dilated cardiomyopathy has a genetic basis.
A. Morales, D. Kinnamon, Elizabeth Jordan, J. Platt, M. Vatta, M. Dorschner, Carl A. Starkey, Jonathan N. Mead, Tomohiko Ai, W. Burke, J. Gastier-Foster, G. Jarvik, H. Rehm, D. Nickerson, R. Hershberger   +14 more
semanticscholar   +1 more source

Psoriasis as risk factor for non-ischemic dilated cardiomyopathy: a population-based cross-sectional study

BMC Cardiovascular Disorders, 2021
Background Psoriasis is a chronic inflammatory skin condition commonly associated with psoriatic arthritis, malignancy, diabetes, inflammatory bowel disease, and cardiovascular disease.
Abbas Alshami, Nasam Alfraji, Steven Douedi, Swapnil Patel, Mohammad Hossain, Deborah Alpert, Dawn Calderon   +6 more
doaj   +1 more source

Dilated cardiomyopathy as the initial presentation of Becker muscular dystrophy: a systematic review of published cases

Orphanet Journal of Rare Diseases, 2022
There are scarce publications regarding the presentation and outcome of Becker muscular dystrophy in adulthood when idiopathic dilated cardiomyopathy is the initial disease manifestation.
Gaspar Del Rio-Pertuz, Cristina Morataya, Kanak Parmar, Sarah Dubay, Erwin Argueta-Sosa   +4 more
doaj   +1 more source

Anaesthetic management of a parturient with dilated cardiomyopathy: A case report

Egyptian Journal of Anaesthesia, 2014
Dilated cardiomyopathy (DCM) is a form of cardiomyopathy characterized by left ventricular or biventricular dilatation and impaired ventricular contractility.
Tarandeep Singh, Susheela Taxak, Neha Hasija, Asha Anand   +3 more
doaj   +1 more source