CASE REPORT
Accepted on 15 May 2025
Cryo-ablation management of atrial fibrillation in Fabry disease without Agalsidase Alpha: a case report
doi 10.3389/fcvm.2025.1483283
- 179 views
- Frontiers in Cardiovascular Medicine
- Cardiovascular Genetics and Systems Medicine
- Research Topics
- Case Reports in Cardiovascular Genetics and Systems Medicine: 2024
Case Reports in Cardiovascular Genetics and Systems Medicine: 2024
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Articles
CASE REPORT
Published on 09 Apr 2025
Case Report: A novel variant of the TTN gene and two other rare variants in a Chinese patient with dilated cardiomyopathy
doi 10.3389/fcvm.2025.1527544
- 591 views
CASE REPORT
Published on 04 Apr 2025
Identification of a novel NKX2-5 variant in a young Ecuadorian patient with atrioventricular block and bradycardia: a case report
doi 10.3389/fcvm.2025.1552423
- 537 views
ORIGINAL RESEARCH
Published on 03 Feb 2025
A case series of patients with cardiac amyloidosis evaluated at a Colombian university hospital
doi 10.3389/fcvm.2025.1487717
- 943 views
CASE REPORT
Published on 20 Jan 2025
Case Report: A case of Tatton-Brown–Rahman syndrome featuring mitral annular disjunction and mitral valve prolapse due to a novel mutation site in the DNMT3A gene
doi 10.3389/fcvm.2024.1507318
- 652 views
CASE REPORT
Published on 20 Jan 2025
Case Report: Rare cardiovascular characteristics of tuberous sclerosis complex with novel TSC2 variant
doi 10.3389/fcvm.2024.1464933
- 678 views
CASE REPORT
Published on 22 Nov 2024
Case Report: Diagnostic challenges in Fabry disease: misinterpreted obstructive hypertrophic cardiomyopathy and the role of enzyme replacement therapy
doi 10.3389/fcvm.2024.1479374
- 826 views
- 1 citation
CASE REPORT
Published on 13 Nov 2024
Case Report: Allelic and biallelic variants in coagulation factor XI cause factor XI deficiency
doi 10.3389/fcvm.2024.1461899
- 702 views
CASE REPORT
Published on 01 Oct 2024
Dilated cardiomyopathy due to novel LMNA mutation: a case report
doi 10.3389/fcvm.2024.1422151
- 1,107 views
CASE REPORT
Published on 06 Sep 2024
Case Report: A Chinese child with Barth syndrome caused by a novel TAFAZZIN mutation
doi 10.3389/fcvm.2024.1465912
- 680 views
CASE REPORT
Published on 25 Jul 2024
Case Report: Patent ductus arteriosus with tuberous sclerosis complex
doi 10.3389/fcvm.2024.1391775
- 681 views
CASE REPORT
Published on 22 May 2024
Case Report: A rare transthyretin mutation p.D58Y in a Chinese case of transthyretin amyloid cardiomyopathy
doi 10.3389/fcvm.2024.1374241
- 974 views
