Cargando…
A Case Report of a Rare Heterozygous Variant in the Desmin Gene Associated With Hypertrophic Cardiomyopathy and Complete Atrioventricular Block
Hypertrophic cardiomyopathy (HCM) is the primary cause of sudden cardiac death in children and adolescents. Patients with HCM frequently have ventricular tachycardia and ventricular fibrillation, although complete atrioventricular block (CAVB) is very rare. We report a case of HCM with CAVB in an 8-...
Autores principales: | Oka, Hideharu, Nakau, Kouichi, Imanishi, Rina, Furukawa, Takuo, Tanabe, Yasuko, Hirono, Keiichi, Hata, Yukiko, Nishida, Naoki, Azuma, Hiroshi |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8531214/ https://www.ncbi.nlm.nih.gov/pubmed/34712946 http://dx.doi.org/10.1016/j.cjco.2021.05.003 |
Ejemplares similares
-
Assessment of Potential Renal Dysfunction in Patients with Congenital Heart Disease after Biventricular Repair
por: Oka, Hideharu, et al.
Publicado: (2018) -
Liver Fibrosis Markers Represent Central Venous Pressure in Post-pubertal Patients With Congenital Heart Disease
por: Oka, Hideharu, et al.
Publicado: (2023) -
Myocardial fibrosis in desmin-related hypertrophic cardiomyopathy
por: He, Yi, et al.
Publicado: (2010) -
Pulmonary Hemodynamic Changes with Nitric Oxide or Oxygen in a Patient with Asplenia, Single Right Ventricle, and Total Anomalous Pulmonary Venous Connection after Fontan Procedure
por: Oka, Hideharu, et al.
Publicado: (2018) -
A Novel NKX2-5 Variant in a Child with Left Ventricular Noncompaction, Atrial Septal Defect, Atrioventricular Conduction Disorder, and Syncope
por: Yamada, Yuya, et al.
Publicado: (2022)