Related Experiment Video
Updated: Jul 24, 2026

07:27
Implantation of Total Artificial Heart in Congenital Heart Disease
Published on: July 18, 2014
Complete heart block in an Inuit family.
1Division of Cardiology, Montreal General Hospital, Quebec.
The Canadian Journal of Cardiology
|October 1, 1988
Summary
This study describes a heritable form of adult-onset complete heart block in an Inuit family. The findings suggest a genetic predisposition to this serious cardiac condition, with affected individuals experiencing syncope.
Area of Science:
- Cardiology
- Genetics
- Indigenous Health
Background:
- Congenital heart block can have genetic origins.
- Familial aggregation of cardiac conduction abnormalities is recognized.
- Previous reports on heritable heart block are limited.
Observation:
- A multi-generational Inuit family from Cape Dorset presented with cardiac conduction abnormalities.
- Six family members had documented complete heart block, one had high-grade atrioventricular block, and one had bi- or trifascicular block.
- All affected individuals experienced syncope; one relative received a pacemaker for unspecified reasons.
Findings:
- Two of three middle-aged relatives exhibited minor conduction abnormalities.
- No conduction problems were observed in younger family members examined.
- This series represents the largest reported cohort of a heritable form of adult-onset complete heart block.
Implications:
- Suggests a genetic basis for adult-onset complete heart block within this population.
- Highlights the importance of family history in diagnosing cardiac conduction disorders.
- Further research into the specific genetic mechanisms is warranted.
More Related Videos
Related Concept Videos
Heart Valves
The human heart is a complex organ with an intricate system of valves that regulate blood flow. There are two main types of valves: atrioventricular (AV) valves and semilunar valves.
The AV valves prevent the backflow of blood from the ventricles to the atria during ventricular contraction. These valves function with the assistance of the chordae tendineae and papillary muscles. When the ventricles are relaxed, the chordae tendineae are slack, allowing blood to flow from the atria into the...
The AV valves prevent the backflow of blood from the ventricles to the atria during ventricular contraction. These valves function with the assistance of the chordae tendineae and papillary muscles. When the ventricles are relaxed, the chordae tendineae are slack, allowing blood to flow from the atria into the...
Disturbances in Heart Rhythm
Arrhythmia or dysrhythmia refers to an abnormal heart rhythm caused by a defect in the heart's conduction system. It can cause the heart to beat irregularly, too quickly, or too slowly, leading to symptoms like chest pain, shortness of breath, and fainting. Factors such as stress, caffeine, alcohol, nicotine, cocaine, certain drugs, congenital defects, diseases, and electrolyte abnormalities can trigger arrhythmias.
Arrhythmias are categorized by their speed, rhythm, and origin. A slow heart...
Arrhythmias are categorized by their speed, rhythm, and origin. A slow heart...
Dysrhythmias IV: Characteristics of Bradyarrhythmias
Bradyarrhythmias are cardiac rhythm disorders characterized by a slower-than-normal heart rate, typically defined as fewer than 60 beats per minute. Some of which are discussed here:Sinus BradycardiaSinus bradycardia presents a heart rate lower than 60 beats per minute, with a regular rhythm originating from the SA node. The ECG typically shows normal P waves preceding each QRS complex, a normal PR interval (0.12 to 0.20 seconds), and a normal QRS duration (0.06 to 0.10 seconds).First-Degree AV...
Dysrhythmias VI: Management of Dysrhythmias
Dysrhythmia management involves a multifaceted approach, incorporating pharmacological treatments, medical procedures, surgical interventions, lifestyle modifications, and patient education.Pharmacological ManagementAntiarrhythmic Drugs:Class I (Sodium Channel Blockers): This class includes quinidine and procainamide, which reduce the speed of impulse conduction in the heart, stabilize the cardiac membrane, and control arrhythmias. Quinidine and procainamide are Class IA agents that prolong the...
Cardiomyopathy III: Hypertrophic Cardiomyopathy
Hypertrophic cardiomyopathy, or HCM, is an autosomal dominant genetic disorder characterized by asymmetric left ventricular hypertrophy without ventricular dilation. It is more common in men and is typically diagnosed in young, athletic adults.EtiologyHCM is primarily genetic and is caused by mutations in genes encoding sarcomeric proteins. Researchers have identified over 1400 mutations across at least 11 different genes. Among these, the most frequently occurring mutations are found in the...

