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Condition: Cardiomyopathy

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Total 870 results found since Jan 2013.

A recurrent homozygous missense DPM3 variant leads to muscle and brain disease
This article is protected by copyright. All rights reserved.PMID:35932216 | DOI:10.1111/cge.14208
Source: Clinical Genetics - August 6, 2022 Category: Genetics & Stem Cells Authors: Sara Nagy Tracy Lau Shahryar Alavi Ehsan Ghayoor Karimiani Jalal Vallian Bobby G Ng Samaneh Noroozi Asl Javad Akhondian Amir Bahreini Omid Yaghini Prech Uapinyoying Carsten Bonnemann Hudson H Freeze Vajira H W Dissanayake Nirmala D Sirisena Miriam Schmidt Source Type: research

Early cardiac rehabilitation after heart transplantation in a patient with limb-girdle muscular dystrophy: A case report
Rationale: Cardiac rehabilitation (CR) after heart transplantation (HT) decreases the mortality rate and increases exercise capacity of patients. Dilated cardiomyopathy develops in most patients with muscular dystrophy (MD), leading to advanced heart failure, necessitating the use of left ventricular assist devices or HT. As the clinical outcomes of left ventricular assist devices and HT in patients with myopathy differ from those in patients without myopathy, CR adapted to patients with MD should be considered. Patient concerns: A 39-year-old man with limb-girdle muscular dystrophy developed dilated cardiomyopa...
Source: Medicine - July 29, 2022 Category: Internal Medicine Tags: Research Article: Clinical Case Report Source Type: research

Acylcarnitines and Genetic Variation in Fat Oxidation Genes in HIV-infected, Antiretroviral-treated Children With and Without Myopathy
Conclusion: FAO appears to be altered in HIV-infected children with and without myopathy, but abnormal FAO does not fully explain myopathy in ARV-exposed children. Further study of SLC22A5 variation in ARV-exposed people is warranted carnitine transporter dysfunction-related cardiomyopathy may be treatable.
Source: The Pediatric Infectious Disease Journal - July 26, 2022 Category: Infectious Diseases Tags: HIV Reports Source Type: research

Surgical Management for Systolic Anterior Motion (SAM) of the Mitral Valve in Obstructive Hypertrophic Myopathy
Ann Thorac Cardiovasc Surg. 2022 Jul 15. doi: 10.5761/atcs.ra.22-00103. Online ahead of print.ABSTRACTIn patients with obstructive hypertrophic cardiomyopathy, left ventricular outflow tract (LVOT) obstruction can be created by the hypertrophic interventricular septum (IVS) as well as systolic anterior motion (SAM) of the anterior mitral leaflet (AML). Sufficient septal myectomy is a fundamental surgical technique to treat LVOT obstruction, however, direct surgical management for SAM is another key aspect. Besides the hypertrophic IVS, mitral valve, subvalvular apparatus, and papillary muscle may play important role for SA...
Source: Annals of Thoracic and Cardiovascular Surgery - July 19, 2022 Category: Cardiovascular & Thoracic Surgery Authors: Akihiko Usui Masato Mutsuga Source Type: research

A clinicopathologic study of malignancy in VCP-associated multisystem proteinopathy
CONCLUSION: This is the first study that expands the phenotype of VCP disease to potentially include rare cancers and highlights the importance of further investigation of the role of VCP in cancer development. The results of this study in VCP disease patients suggest that patients may be at an increased risk for rare tumors. A larger study will determine if patients with VCP disease develop cancer at a higher rate than the general population. If that is the case, they should be followed up more frequently and screened for recurrence and metastasis of their cancer.PMID:35841038 | DOI:10.1186/s13023-022-02403-9
Source: Cancer Control - July 15, 2022 Category: Cancer & Oncology Authors: Alyaa Shmara Mari Perez-Rosendahl Kady Murphy Ashley Kwon Charles Smith Virginia Kimonis Source Type: research

A case of congenital fiber-type disproportion syndrome presenting dilated cardiomyopathy with ACTA1 mutation
CONCLUSION: Apoptosis induced in Met327Lys-transfected muscle cells supports the pathogenicity of the mutation and can be implicated as one of the histopathological features associated with CFTD, as in NM.PMID:35757965 | DOI:10.1002/mgg3.2008
Source: Molecular Medicine - June 27, 2022 Category: Molecular Biology Authors: Ayumi Matsumoto Hidetoshi Tsuda Sadahiro Furui Masako Kawada-Nagashima Tatsuya Anzai Mitsuru Seki Kazuhisa Watanabe Kazuhiro Muramatsu Hitoshi Osaka Sadahiko Iwamoto Ichizo Nishino Takanori Yamagata Source Type: research