Literature DB >> 10431113

Familial clustering of infantile cirrhosis in Northern Germany: A clue to the etiology of idiopathic copper toxicosis.

T Müller1, H Schäfer, B Rodeck, G Haupt, H Koch, H Bosse, P Welling, H Lange, R Krech, D Feist, K E Mühlendahl, J Brämswig, H Feichtinger, W Müller.   

Abstract

Two cases of infantile liver cirrhosis of unknown origin occurred in a circumscribed rural area of Northern Germany. Both children had increased dietary copper exposure. The search for additional cases of what appeared to be idiopathic copper toxicosis (ICT) revealed a cluster of affected infants in this region, raising questions about the relative importance of genetic and environmental factors that are considered to be etiologic. We gathered clinical and pathologic data concerning the patients, analyzed the pedigrees of affected families, and searched for possible environmental factors contributing to the pathologic process. We encountered 8 cases of infantile liver cirrhosis in 5 families in Emsland, a circumscribed and predominantly rural area of Northern Germany; ICT was definitely proven in 2 cases. Clinical presentation and liver pathology in 6 additional cases were consistent with the diagnosis of ICT. Pedigrees of affected families revealed complex relationships with occasional consanguinity of parents, suggesting autosomal recessive inheritance. The households were served by private wells with water of low pH flowing through copper pipes, suggesting the possibility of increased alimentary copper exposure. These findings support earlier conclusions that ICT develops when an infant with a genetic predisposition is exposed to a copper-enriched diet.

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Year:  1999        PMID: 10431113     DOI: 10.1016/s0022-3476(99)70021-1

Source DB:  PubMed          Journal:  J Pediatr        ISSN: 0022-3476            Impact factor:   4.406


  4 in total

1.  Idiopathic copper toxicosis: is abnormal copper metabolism a primary cause of this disease?

Authors:  Masaru Harada; Yuichi Honma; Tomoharu Yoshizumi; Keiichiro Kumamoto; Shinji Oe; Noboru Harada; Aya Tanimoto; Kei Yabuki; Tsukasa Karasuyama; Akitoshi Yoneda; Michihiko Shibata
Journal:  Med Mol Morphol       Date:  2019-06-03       Impact factor: 2.309

Review 2.  Molecular pathogenesis of Wilson and Menkes disease: correlation of mutations with molecular defects and disease phenotypes.

Authors:  P de Bie; P Muller; C Wijmenga; L W J Klomp
Journal:  J Med Genet       Date:  2007-08-23       Impact factor: 6.318

Review 3.  Liver tumors in children with metabolic disorders.

Authors:  Deborah A Schady; Angshumoy Roy; Milton J Finegold
Journal:  Transl Pediatr       Date:  2015-10

Review 4.  Copper Toxicity Is Not Just Oxidative Damage: Zinc Systems and Insight from Wilson Disease.

Authors:  R G Barber; Zoey A Grenier; Jason L Burkhead
Journal:  Biomedicines       Date:  2021-03-20
  4 in total

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