Literature DB >> 24266916

Metal storage disorders: Wilson disease and hemochromatosis.

Pushpjeet Kanwar1, Kris V Kowdley.   

Abstract

Hereditary hemochromatosis and Wilson disease are autosomal recessive storage disorders of iron and copper overload, respectively. These metals are involved in multiple redox reactions, and their abnormal accumulation can cause significant injury in the liver and other organs. Over the last few decades clinicians have developed a much better understanding of these metals and their mechanism of action. Moreover, sophisticated molecular genetic testing techniques that make diagnostic testing less invasive are now available. This article updates and discusses the pathogenesis, diagnosis, and management of these metal storage disorders.
Copyright © 2014 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Cirrhosis; Copper; Ferritin; Hemochromatosis; Hepcidin; Wilson disease

Mesh:

Substances:

Year:  2013        PMID: 24266916     DOI: 10.1016/j.mcna.2013.09.008

Source DB:  PubMed          Journal:  Med Clin North Am        ISSN: 0025-7125            Impact factor:   5.456


  7 in total

Review 1.  Recent advances in hemochromatosis: a 2015 update : a summary of proceedings of the 2014 conference held under the auspices of Hemochromatosis Australia.

Authors:  Dilum Ekanayake; Clinton Roddick; Lawrie W Powell
Journal:  Hepatol Int       Date:  2015-03-12       Impact factor: 6.047

2.  Ecotoxicological impacts of industrial effluents on irrigation water quality, animal health and the role of calcium alginate in effluents treatment.

Authors:  Hanaa Abdel Atty Zeid; Moustafa Mohsen El-Zayat; Abeer El-Said Abdrabouh
Journal:  Environ Monit Assess       Date:  2022-07-15       Impact factor: 3.307

3.  Biochemical studies on the effect of different water resources in Hail region on liver and kidney functions of rats.

Authors:  Ola F A Talkhan; Safaa A E Abd Elwahab; Ebtessam M Shalapy
Journal:  Environ Monit Assess       Date:  2016-07-26       Impact factor: 2.513

4.  Iron promotes protein insolubility and aging in C. elegans.

Authors:  Ida M Klang; Birgit Schilling; Dylan J Sorensen; Alexandria K Sahu; Pankaj Kapahi; Julie K Andersen; Peter Swoboda; David W Killilea; Bradford W Gibson; Gordon J Lithgow
Journal:  Aging (Albany NY)       Date:  2014-11       Impact factor: 5.682

5.  The risk of new-onset cancer associated with HFE C282Y and H63D mutations: evidence from 87,028 participants.

Authors:  Yang-Fan Lv; Xian Chang; Rui-Xi Hua; Guang-Ning Yan; Gang Meng; Xiao-Yu Liao; Xi Zhang; Qiao-Nan Guo
Journal:  J Cell Mol Med       Date:  2016-02-19       Impact factor: 5.310

6.  Population genomics in South East Asia captures unexpectedly high carrier frequency for treatable inherited disorders.

Authors:  Yasmin Bylstra; Jyn Ling Kuan; Weng Khong Lim; Jaydutt Digambar Bhalshankar; Jing Xian Teo; Sonia Davila; Bin Tean Teh; Steve Rozen; Ene-Choo Tan; Wendy Kein Meng Liew; Khung Keong Yeo; Patrick Tan; Seang Mei Saw; Ching-Yu Cheng; Stuart Cook; Roger Foo; Saumya Shekhar Jamuar
Journal:  Genet Med       Date:  2018-07-02       Impact factor: 8.822

Review 7.  New perspectives on oxidized genome damage and repair inhibition by pro-oxidant metals in neurological diseases.

Authors:  Joy Mitra; Erika N Guerrero; Pavana M Hegde; Haibo Wang; Istvan Boldogh; Kosagi Sharaf Rao; Sankar Mitra; Muralidhar L Hegde
Journal:  Biomolecules       Date:  2014-07-17
  7 in total

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