Juvenile Hemochromatosis C0268060
A genetic disorder causing excess iron to build up in organs, affecting children and teens. Treatment includes phlebotomy and dietary changes to prevent organ damage.
Key facts at a glance
- ICD-10
- E88.9
- ICD-11
- 5A00.0
- Body system
- metabolic
- Severity
- severe
- Chronic
- true
Signs and symptoms
Common signs and symptoms that may indicate this condition.
Fatigue
(metabolic)Fatigue or weight changes
(metabolic)Significant symptoms that substantially affect daily functioning.
Frequency: Common at all stages
Joint pain
(metabolic)Bronze skin
(metabolic)Cardiomyopathy
(metabolic)Diagnosis and tests
How this condition is diagnosed and what test results mean.
Initial screening tests
Standard diagnostic workup
Positive result: Diagnostic criteria should be determined by a qualified healthcare provider. [Content pending medical review.]
Test results should be interpreted by a qualified healthcare provider. [Content pending medical review.]
Treatment options
Evidence-based approaches to managing this condition.
First-line treatments
Pharmacological management with first-line agents
Active treatment with regular monitoring by a healthcare provider is recommended.
Therapeutic phlebotomy
Regular therapeutic blood removal to deplete iron stores, which is the primary treatment for juvenile hemochromatosis to prevent organ damage.
Iron chelation therapy
Chelating agents such as deferoxamine or deferasirox for patients who cannot tolerate phlebotomy, working to bind and eliminate excess iron through urine and feces.
Additional treatment options
Iron-restricted diet counseling
Dietary modification to limit iron intake, avoiding iron-fortified foods, red meat, and vitamin C supplements that enhance iron absorption.
dietaryIron studies and organ function monitoring
Regular laboratory monitoring of serum ferritin, transferrin saturation, and hepatic function to track treatment response and prevent iron-related organ damage.
monitoringAntioxidant supplementation support
Adjunctive antioxidant therapy including vitamin E and other supplements to help protect organs from iron-induced oxidative damage.
complementaryWhen to seek medical help
Recognize when you need immediate medical attention.
See a doctor within 24 hours
Moderate to severe symptoms that may indicate worsening of this condition. Prompt medical evaluation is recommended.
Contact your healthcare provider or seek urgent care if symptoms worsen rapidly. Go to the emergency department for life-threatening symptoms.
Frequently asked questions
Common questions about this topic.
What is Juvenile Hemochromatosis C0268060?
Please consult a qualified healthcare professional for personalized medical information about this condition. [Content pending medical review.]
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This content is for general informational and educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment. Always seek the guidance of a qualified healthcare provider with any questions you have about a medical condition, and never disregard professional medical advice or delay seeking it because of something you read here.
If you think you may have a medical emergency, call your local emergency number or go to the nearest emergency department immediately.
Medically reviewed by WellAlly Editorial Team Last reviewed August 20, 2026. · Read our editorial policy