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CASE REPORT

Poor cognitive development and abdominal pain: Wilson's disease

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Pages 361-364 | Received 03 Feb 2005, Published online: 08 Jul 2009

References

  • Wilson SAK. Progressive lenticular degeneration: a familial nervous disease associated with cirrhosis of the liver. Brain 1912; 34: 295–509
  • Scheinberg IH, Sternlieb I.. Wilson's disease. WB Saunders, Philadelphia 1984
  • Goldstein NP, Ewert MA, Randall RV, Gross JB. Psychiatric aspects of Wilson's disease (hepatolenticular degeneration). Results of psychometric tests during long-term therapy. Am J Psychiatry 1968; 124: 1555–61
  • Bull PC, Thomas GR, Rommens JM, Forbes JR, Cox DW. The Wilson's disease gene is a putative copper transporting P-type ATPase similar to the Menkes gene. Nat Genet 1993; 5: 327–37
  • Tanzi RE, Petrukhin K, Chernov I, Pellequer JL, Wasco W, Ross B, et al. The Wilson disease gene is a copper transporting ATPase with homology to the Menkes disease gene. Nat Genet 1993; 5: 44–50
  • Nagano K, Nakamura K, Urakami KI, Umeyama K, Uchiyama H, et al. Intracellular distribution of the Wilson's disease gene product (ATPase/B) after in vitro and in vivo exogenous expression in hepatocytes from the LEC rat, an animal model of Wilson's disease. Hepatology 1998; 27: 799–807
  • Gu M, Cooper JM, Butler P, Walker AP, Mistry PK, Dooley JS, et al. Oxidative-phosphorylation defects in liver of patients with Wilson's disease. Lancet 2000; 356: 469–74
  • Carlson MD, Al-Mateen M, Brewer GJ. Atypical childhood Wilson's disease. Pediatr Neurol 2004; 30: 57–60
  • Staatci I, Topcu M, Baltaoglu FF, Köse G, Yalaz K, Renda Y, et al. Cranial MR findings in Wilson's disease. Acta Radiol 1997; 38: 250–8
  • Frydman MB, Bonne-Tamir LA, Farrer PM, Conneally A, Magazanik A, Asknel S, et al. Assignment of the gene for Wilson's disease to chromosome 13. Linkage to the esterase D locus. Proc Natl Acad Sci USA 1985; 82: 1819–21
  • Palsson R, Jonasson JG, Kristjansson M, Bodvardsson A, Goldin RD, Cox DW, et al. Genotype-phenotype interactions in Wilson's disease: insight from an Icelandic mutation. Eur J Gantroenterol Hepatol 2001; 13: 433–6
  • Olsson C, Waldenstrom E, Westermark K, Landegre U, Syvanen AC. Determination of the frequencies of the allelic variants of the Wilson disease gene (ATP7B) in pooled DNA samples. Eur J Hum Genet 2000; 8: 933–8
  • Huster D, Weizenegger M, Kress S, Mossner J, Caca K. Rapid detection of mutations in Wilson disease gene ATP7B by DNA strip technology. Clin Chem Lab Med. 2004; 42: 507–10
  • Walshe JM. Penicillamine, a new oral therapy for Wilson's disease. Am J Med 1956; 21: 487–95
  • Tanner S. Disorders of copper metabolism. Diseases of the liver and biliary system in children, D Kelly. Blackwell Publishing, Oxford 2004; 243–58
  • Brewer GJ, Dick RD, Johnson VD, Fink JK, Kluin KJ, Daniels S. Treatment of Wilson's disease with zinc XVI: treatment during the pediatric years. Gut 2001; 48: 849–52

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