How Dr. Rishi Chadha Diagnoses Hemochromatosis?
Dr. Chadha uses a clear, step-by-step approach:
Medical & Family History
Reviews your personal health, symptoms and family history to assess hereditary risk.
Blood Tests
Orders serum ferritin and transferrin saturation to measure iron stores and transport.
Genetic Testing
Performs HFE gene analysis to identify common mutations linked to hemochromatosis.
Imaging or Biopsy
Uses MRI-based iron quantification or, if needed, liver biopsy to evaluate organ iron loading.
Confirmation & Planning
Integrates all results to confirm iron overload and tailor your treatment plan.
Frequently Asked Questions
What causes hereditary hemochromatosis?
A gene mutation in the HFE gene causes the body to absorb and store too much iron.
What is the ICD-10 code?
Primary hemochromatosis is coded as E83.11.
How do doctors diagnose it?
Through blood tests (serum ferritin, transferrin saturation), genetic testing for HFE mutations, and, if needed, imaging or liver biopsy.
Can women get hemochromatosis?
Yes. Women often develop symptoms later than men, sometimes manifesting as irregular periods or early menopause.
Is it dangerous if untreated?
Yes. Excess iron can damage the liver, heart, pancreas, joints, and other organs.
How often is phlebotomy needed?
Initially, weekly phlebotomy is common. Maintenance sessions are less frequent once iron levels normalize.
Can I manage it with diet alone?
No. While dietary changes help limit iron intake, medical treatments like phlebotomy or chelation are required to remove excess iron.
Is phlebotomy safe?
Yes. It's a quick, safe procedure. You may feel light-headed, and Dr. Chadha monitors you throughout.
Should I get genetic testing?
Yes. Genetic testing confirms hereditary risk, guides family screening, and helps tailor your care plan.