- Email: info@hyperinsulinism-india.org
Raising a child with CHI can be overwhelming, especially right after diagnosis. Our downloadable guides provide families with practical, easy-to-understand information to help navigate treatment, daily care, and long-term management.
What you’ll find:
Early detection and expert care are critical to preventing complications from CHI. We provide up-to-date clinical references and tools for pediatricians, neonatologists, endocrinologists, and general practitioners.
Includes:
Have questions about CHI? You're not alone. Here are answers to the most common ones asked by families and newly diagnosed patients.
Congenital Hyperinsulinism (CHI) is caused by genetic mutations that lead the pancreas to produce too much insulin. The most common gene mutations are in ABCC8 and KCNJ11, which affect how insulin is released. These mutations can be inherited from one or both parents.
While there is no universal cure, CHI can often be effectively managed through medications, dietary strategies, and in some cases, surgery. Some children outgrow the condition as they age, while others require long-term care.
es, if left untreated, CHI can lead to dangerously low blood sugar levels, resulting in seizures, brain damage, or even death. However, with early diagnosis and proper treatment, children with CHI can live healthy, fulfilling lives.
Treatment depends on the severity and type of CHI. It may include:
With appropriate care, most children with CHI can attend school, play, and grow normally. Some may require long-term management, but many lead active, healthy lives.
If CHI is inherited in an autosomal recessive pattern, each sibling has a 25% chance of having the condition. Genetic counseling and testing can help determine the risk for future pregnancies.
