Hereditary Liver Diseases: Wilson's Disease and Hemochromatosis

被引：2

作者：

Merle, Uta ^{[1
,4
]}

Mohr, Isabelle ^{[2
,3
]}

机构：

[1] Univ Klinikum Heidelberg, Sekt Transplantat Hepatol Inneren Med 4, Heidelberg, Germany

[2] Univ Klin Mainz, Viszeral & Transplantat Chirurg, Mainz, Germany

[3] Univ Klinikum Heidelberg, Med Klin 4, Heidelberg, Germany

[4] Univ Klinikum Heidelberg, Abt Gastroenterol Infekt Krankheiten & Vergiftunge, Neuenheimer Feld 410, D-69120 Heidelberg, Germany

来源：

DEUTSCHE MEDIZINISCHE WOCHENSCHRIFT | 2023年 / 148卷 / 13期

关键词：

hemochromatosis; Wilson's disease; iron-overload; copper-overload; DIAGNOSIS;

D O I：

10.1055/a-1871-6393

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

[No abstract available]

引用

页码：836 / 843

页数：8

共 11 条

[1] Worse Outcomes of Patients With HFE Hemochromatosis With Persistent Increases in Transferrin Saturation During Maintenance Therapy [J].

Bardou-Jacquet, Edouard ;

Laine, Fabrice ;

Guggenbuhl, Pascal ;

Morcet, Jeff ;

Jezequel, Caroline ;

Guyader, Dominique ;

Moirand, Romain ;

Deugnier, Yves .

CLINICAL GASTROENTEROLOGY AND HEPATOLOGY, 2017, 15 (10) :1620-1627

[2] Wilson disease [J].

Czlonkowska, Anna ;

Litwin, Tomasz ;

Dusek, Petr ;

Ferenci, Peter ;

Lutsenko, Svetlana ;

Medici, Valentina ;

Rybakowski, Janusz K. ;

Weiss, Karl Heinz ;

Schilsky, Michael L. .

NATURE REVIEWS DISEASE PRIMERS, 2018, 4

[3] Diagnosis and phenotypic classification of Wilson disease [J].

Ferenci, P ;

Caca, K ;

Loudianos, G ;

Mieli-Vergani, G ;

Tanner, S ;

Sternlieb, I ;

Schilsky, M ;

Cox, D ;

Berr, F .

LIVER INTERNATIONAL, 2003, 23 (03) :139-142

[4] Age and Sex but Not ATP7B Genotype Effectively Influence the Clinical Phenotype of Wilson Disease [J].

Ferenci, Peter ;

Stremmel, Wolfgang ;

Czlonkowska, Anna ;

Szalay, Ferenc ;

Viveiros, Andre ;

Staettermayer, Albert Friedrich ;

Bruha, Radan ;

Houwen, Roderick ;

Pop, Tudor Lucian ;

Stauber, Rudolf ;

Gschwantler, Michael ;

Pfeiffenberger, Jan ;

Yurdaydin, Cihan ;

Aigner, Elmar ;

Steindl-Munda, Petra ;

Dienes, Hans-Peter ;

Zoller, Heinz ;

Weiss, Karl Heinz .

HEPATOLOGY, 2019, 69 (04) :1464-1476

[5]

Ferenci P, 2012, J HEPATOL, V56, P671, DOI 10.1016/j.jhep.2011.11.007

[6] Noninvasive prediction of fibrosis in C282Y homozygous hemochromatosis [J].

Guyader, D ;

Jacquelinet, C ;

Moirand, R ;

Turlin, B ;

Mendler, MH ;

Chaperon, J ;

David, V ;

Brissot, P ;

Adams, P ;

Deugnier, Y .

GASTROENTEROLOGY, 1998, 115 (04) :929-936

[7] ACG Clinical Guideline: Hereditary Hemochromatosis [J].

Kowdley, Kris V. ;

Brown, Kyle E. ;

Ahn, Joseph ;

Sundaram, Vinay .

AMERICAN JOURNAL OF GASTROENTEROLOGY, 2019, 114 (08) :1202-1218

[8] Clinical presentation, diagnosis and long-term outcome of Wilson's disease: a cohort study [J].

Merle, U. ;

Schaefer, M. ;

Ferenci, P. ;

Stremmel, W. .

GUT, 2007, 56 (01) :115-120

[9] Haemochromatosis [J].

Powell, Lawrie W. ;

Seckington, Rebecca C. ;

Deugnier, Yves .

LANCET, 2016, 388 (10045) :706-716

[10] A multidisciplinary approach to the diagnosis and management of Wilson disease: 2022 practice guidance on Wilson disease from the American Association for the Study of Liver Diseases [J].

Schilsky, Michael L. ;

Roberts, Eve A. ;

Bronstein, Jeff M. ;

Dhawan, Anil ;

Hamilton, James P. ;

Rivard, Anne Marie ;

Washington, Mary Kay ;

Weiss, Karl Heinz ;

Zimbrean, Paula C. .

HEPATOLOGY, 2022,

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