Juvenile hemochromatosis
Juvenile hemochromatosis (ju·ve·nile - he·mo·chro·ma·to·sis) is a condition that is present at birth (congenital), but is typically not diagnosed until later in life. Hemochromatosis is, however, sometimes diagnosed between the ages of 15 and 30. This is known as juvenile hemochromatosis.
What is juvenile hemochromatosis?
Hemochromatosis is an inherited condition that causes the body to absorb too much iron from foods.

What are the signs and symptoms of juvenile hemochromatosis?
Early symptoms
Cansancio
Dolor en el abdomen
Pain in the joints
Debilidad
Later symptoms
Problems with sexual function
How is juvenile hemochromatosis diagnosed?
Hemochromatosis is a condition that is present at birth (congenital), but is typically not diagnosed until later in life – generally around age 50 or 60. Hemochromatosis is, however, sometimes diagnosed between the ages of 15 and 30. This is known as juvenile hemochromatosis.
In a person with this condition, the body absorbs too much iron from foods. In turn, that extra iron is stored in the organs, including the liver, heart and pancreas. Extra iron in these organs can cause serious problems, such as liver disease, heart problems and diabetes.
What are the causes of juvenile hemochromatosis?
Hemochromatosis is hereditary (passed down in families) through a mutated gene.
Juvenile hemochromatosis doctors and providers
- Dra. Amal Aqul, MDHepatóloga pediátrica
- Dra. Megha Mehta, MDGastroenteróloga pediátrica
- Dra. Charina Ramirez, MDGastroenteróloga pediátrica
- Dr. Norberto Rodriguez-Baez, MDHepatólogo pediátrico
- Dra. Isabel Rojas Santamaria, MDGastroenteróloga pediatra
- Prof. Phuong Luu, PA-CAsistente médico: Gastroenterología
- To Nhu Nguyen, PA-CPhysician Assistant - Gastroenterology
- Prof. Jennifer Peacock, APRN, PNP-PCEnfermera facultativa pediátrica: Gastroenterología
- Prof. Shabina Walji-Virani, APRN, PNP-PCEnfermera facultativa pediátrica: Gastroenterología