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Case Reports
. 2022 Jan;28(1):131-133.
doi: 10.1002/lt.26263. Epub 2021 Sep 18.

Pseudo-Wilsonian Crisis in a ATP7B Heterozygote

Mohammad Qasim Khan  1 , Jerry Yung-Lun Chin, Hassan Azhari, Charles B Rosen, Michael D Leise
Affiliations
Case Reports

Pseudo-Wilsonian Crisis in a ATP7B Heterozygote

Mohammad Qasim Khan et al. Liver Transpl. 2022 Jan.
No abstract available

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References

    1. Roy S, McCann CJ, Ralle M, Ray K, Ray J, Lutsenko S, Jayakanthan S. Analysis of Wilson disease mutations revealed that interactions between different ATP7B mutants modify their properties. Sci Rep 2020;10:13487.
    1. van den Berghe PV, Klomp LW. New developments in the regulation of intestinal copper absorption. Nutr Rev 2009;67:658–672.
    1. Taylor AA, Tsuji JS, Garry MR, McArdle ME, Goodfellow WL Jr., Adams WJ, Menzie CA. Critical review of exposure and effects: implications for setting regulatory health criteria for ingested copper. Environ Manage 2020;65:131–159.
    1. Stapelbroek JM, Bollen CW, Ploos van Amstel JK, van Erpecum KJ, van Hattum J, van den Berg LH, et al. The H1069Q mutation in ATP7B is associated with late and neurologic presentation in Wilson disease: results of a meta‐analysis. J Hepatol 2004;41:758–763.
    1. Brewer GJ. Editorial: Is heterozygosity for a Wilson’s disease gene defect an important underlying causes of infantile and childhood copper toxicosis syndromes? J Trace Elem Exp Med 2000;13:249–254.

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