Teaching Plan: Hereditary haemochromatosis

Hereditary haemochromatosis (HH) is a common genetic disorder in Australia, affecting one in 200 people of European descent, which can lead to iron overload and serious health complications if untreated. GP registrars should develop an evidence-based approach to diagnosing and managing HH, including when to utilise genetic testing.

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Date reviewed: 06 December 2024

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