CASE REPORT
Published on 23 Jun 2025
The genomic bases of atrial fibrillation in an Ecuadorian patient: a case report
doi 10.3389/fcvm.2025.1552417
- 1,119 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
5,950
Total downloads
23k
Total views and downloads
Articles
CASE REPORT
Published on 13 Jun 2025
Genetic mutation and blue rubber bleb nevus syndrome: case reports and literature review
doi 10.3389/fgene.2025.1516562
- 982 views
CASE REPORT
Published on 30 May 2025
Cryo-ablation management of atrial fibrillation in Fabry disease without agalsidase alpha: a case report
doi 10.3389/fcvm.2025.1483283
- 1,174 views
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
- 1,338 views
- 1 citation
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
- 993 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
- 1,414 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
- 1,048 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
- 1,032 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
- 1,247 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
- 992 views
CASE REPORT
Published on 01 Oct 2024
Dilated cardiomyopathy due to novel LMNA mutation: a case report
doi 10.3389/fcvm.2024.1422151
- 1,625 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
- 965 views
