Results 21 to 30 of about 145,091 (327)

Molecular studies in familial dilated cardiomyopathy – A pilot study

International Journal of Cardiology: Heart & Vasculature, 2022
Aim: To study genetic variants in patients of familial dilated cardiomyopathy. Methodology: Patients with reduced ejection fraction of less than 45% and dilated left ventricle are considered to have dilated cardiomyopathy.
Vyom Mori, J.P.S. Sawhney, I.C. Verma, Ashwani Mehta, Renu Saxena, Rajiv Passey, Arun Mohanty, Bhuwanesh Kandpal, B.S. Vivek, Manish Sharma, Ashish Kumar Jain, Dipak Katare   +11 more
doaj   +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

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

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

Non-compaction cardiomyopathy – brief review [PDF]

, 2017
Left ventricular non-compaction cardiomyopathy is a genetic disorder characterized by the presence of two myocardial layers with numerous prominent trabeculations and deep inter-trabecular recesses that communicate with the ventricular cavity.
Berceanu, Mihaela, Constantin, Anca, Donoiu, Ionuț, Istrătoaie, Octavian, Militaru, Constantin, Mirea, Oana, Mănescu, Mirela, Târtea, Georgică Costinel   +7 more
core   +3 more sources

Cardiomyopathy, familial dilated [PDF]

Orphanet Journal of Rare Diseases, 2006
AbstractDilated cardiomyopathy (DCM) is a heart muscle disease characterized by ventricular dilatation and impaired systolic function. Patients with DCM suffer from heart failure, arrhythmia, and are at risk of premature death. DCM has a prevalence of one case out of 2500 individuals with an incidence of 7/100,000/year (but may be under diagnosed).
Mestroni Luisa, Carniel Elisa, Taylor Matthew RG   +2 more
openaire   +3 more sources

Genetics of Dilated Cardiomyopathy

Annual Review of Medicine, 2021
Dilated cardiomyopathy (DCM) is defined as dilation and/or reduced function of one or both ventricles and remains a common disease worldwide. An estimated 40% of cases of familial DCM have an identifiable genetic cause. Accordingly, there is a fast-growing interest in the field of molecular genetics as it pertains to DCM. Many gene mutations have been
Ramone, Eldemire, Luisa, Mestroni, Matthew R G, Taylor   +2 more
openaire   +3 more sources

Familial dilated cardiomyopathy [PDF]

Heart, 1994
ardiomyopathies are diseasesof the heart muscle that renderthe heart unable to properlypump enough blood to the body. In thedilated form of cardiomyopathy(called dilated cardiomyopathy orDCM), the heart is enlarged (Figure 1).As the heart enlarges, it becomes lesseffective in pumping blood, whichthen leads to symptoms of heart failureand irregular ...
L. Mestroni, M. Krajinovic, G. M. Severini, B. Pinamonti, A. D. Lenarda, GIACCA, MAURO, A. Falaschi, F. Camerini   +7 more
openaire   +3 more sources

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

Peripartum cardiomyopathy: diagnosis and management [PDF]

, 2017
No abstract ...
Coats, Caroline J., Dalzell, Jonathan R., Jackson, Alice M., Jhund, Pardeep S., Petrie, Mark C., Walker, Niki L.   +5 more
core   +1 more source