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. 2023 Mar 15;14(4):282-286.
doi: 10.1136/flgastro-2022-102296. eCollection 2023.

European Association for Study of the Liver (EASL) clinical practice guidelines on haemochromatosis

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European Association for Study of the Liver (EASL) clinical practice guidelines on haemochromatosis

Jennifer Cathcart et al. Frontline Gastroenterol. .

Abstract

The European Association for the Study of the Liver has recently updated guidance on haemochromatosis with a more extensive discussion on investigation and management.[ The new guidance focuses on non-invasive methods for fibrosis assessment and early diagnosis to include more extensive genetic testing if needed. Early diagnosis and treatment is vital as it reduces morbidity and mortality. We review this guideline and offer key updated messages with a focus on new developments since the last guidance and key aspects of current practice.

Keywords: HAEMOCHROMATOSIS; LIVER; LIVER CIRRHOSIS.

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Conflict of interest statement

Competing interests: None declared.

Figures

Figure 1
Figure 1
Algorithm for diagnosis of suspected haemochromatosis. *Rare genetic testing to include at minimum HFE, HAMP, HJV, TFR2, SCL40A1, BMP6, CP and TF.

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References

    1. European Association for the Study of the Liver. Electronic address: easloffice@easloffice.eu, European Association for the Study of the Liver . EASL clinical practice guidelines on haemochromatosis. J Hepatol 2022;77:479–502. 10.1016/j.jhep.2022.03.033 - DOI - PubMed
    1. Haemochromatosis UK . Diagnosis and care. Available: www.haemochromatosis.org.uk/diagnosis-and-care-by-gps [Accessed Aug 2022].
    1. Pilling LC, Tamosauskaite J, Jones G, et al. . Common conditions associated with hereditary haemochromatosis genetic variants: cohort study in UK Biobank. BMJ 2019:k5222. 10.1136/bmj.k5222 - DOI - PMC - PubMed
    1. Allen KJ, Gurrin LC, Constantine CC, et al. . Iron-overload-related disease in HFE hereditary hemochromatosis. N Engl J Med 2008;358:221–30. 10.1056/NEJMoa073286 - DOI - PubMed
    1. Whitlock EP, Garlitz BA, Harris EL, et al. . Screening for hereditary hemochromatosis: a systematic review for the U.S. preventive services task force. Ann Intern Med 2006;145:209–23. 10.7326/0003-4819-145-3-200608010-00009 - DOI - PubMed

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