Congenital Hypertrophic Disease refers to a group of conditions present at birth where there is abnormal thickening (hypertrophy) of tissues, muscles, or organs, often affecting the heart, digestive system, or skeletal muscles. The most commonly known form is Congenital Hypertrophic Cardiomyopathy, a condition where the heart muscles become abnormally thick, making it harder for the heart to pump blood efficiently.
Congenital Hypertrophic Disease usually occurs due to genetic mutations passed from one or both parents. It can also be associated with certain metabolic or developmental disorders that influence tissue growth before birth. Common risk factors include:
Symptoms may vary depending on the organ involved, but common signs include:
Early diagnosis is crucial for effective management. Our advanced diagnostic facilities include:
While there’s no permanent cure, timely intervention helps manage symptoms and prevent complications. Treatment plans are tailored based on the child’s condition and may include:
At our center, we combine cutting-edge diagnostic technology with personalized care to ensure the best outcomes for children born with Congenital Hypertrophic Disease. Our team of experienced pediatric cardiologists, genetic specialists, and surgeons work together to provide comprehensive diagnosis, treatment, and long-term follow-up care.