Related Experiment Video
Updated: Aug 19, 2026

Measuring Cardiac Autonomic Nervous System (ANS) Activity in Children
Published on: April 29, 2013
Cardiomyopathy in children in Ahmedabad
V K Gandhi1, S B Dalal, J R Sharma
1Department of Pediatrics, K.M. School of Post-graduates, V.S. General Hospital, Ahmedabad.
Insights
Pediatric cardiomyopathies, including dilated (DCM), restrictive (RCM), and hypertrophic (HCM), are most common in children aged 2-5 and 10-16 years. Despite treatment, advanced cases show a poor prognosis.
Area of Science:
- Pediatric Cardiology
- Cardiovascular Research
- Clinical Pediatrics
Background:
- Cardiomyopathies are a significant cause of heart disease in children.
- Understanding the epidemiology and clinical presentation of pediatric cardiomyopathies is crucial for timely diagnosis and management.
- Dilated cardiomyopathy (DCM), restrictive cardiomyopathy (RCM), and hypertrophic cardiomyopathy (HCM) are key types affecting the pediatric population.
Purpose of the Study:
- To present a clinical study and follow-up of 20 children with various cardiomyopathies up to age 16.
- To describe the common types of cardiomyopathy in the pediatric age group.
- To outline the clinical presentation and prognosis of pediatric cardiomyopathies.
Main Methods:
- A clinical study involving 20 children diagnosed with cardiomyopathy.
- Follow-up of patients up to 16 years of age.
- Analysis of clinical presentations and treatment responses.
Main Results:
- Dilated cardiomyopathy (DCM) was the most common type, followed by restrictive cardiomyopathy (RCM) and hypertrophic cardiomyopathy (HCM).
- Short-chain hydroxyacyl-CoA dehydrogenase deficiency (SHMD) presenting with cardiomyopathy was frequent in infancy and early childhood.
- Cardiomyopathies most frequently presented between ages 2-5 and 10-16 years, with DCM showing near-equal distribution across these groups.
Conclusions:
- Cardiomyopathies in children exhibit distinct age distributions for different types.
- Clinical presentation varies among cardiomyopathy subtypes.
- Despite aggressive treatment, advanced pediatric cardiomyopathies often have a rapidly downhill course and a poor general prognosis.
Abstract:
A clinical study and follow up of 20 children with cardiomyopathies upto age of 16 years are presented. The DCM was most common variety followed by RCM and HCM in pediatric age group. SHMD presenting with cardiomyopathy were common in infancy and early childhood. Cardiomyopathies presented most frequently between 2-5 years and 10-16 years age group with DCM having almost equal distribution. Clinical presentation of various types is described, despite of vigorous decongestive and vasodilator treatment in advanced cases, course was rapidly downhill and prognosis is poor in general.
More Related Videos
Related Concept Videos
Cardiomyopathy I: Introduction and Classification
Cardiomyopathy II: Dilated Cardiomyopathy
Cardiomyopathy III: Hypertrophic Cardiomyopathy
Cardiomyopathy IV: Restrictive Cardiomyopathy
Cardiomyopathy V: Interprofessional Care
Cardiomyopathy VI: Nursing Management

