Wilson disease

Wilson disease is a very rare inherited multisystemic disease presenting non-specific neurological, hepatic, psychiatric or osseo-muscular manifestations due to excessive copper deposition in the body.

Thrombocytopenia

A reduction in the number of circulating thrombocytes.


Total: 4

                       


(per page)
PMID (PMCID)
25617103
 FEMALE
Wilson disease with thrombocytopenia (case report).
Zhvania M, Gogberashvili K, Gagoshidze M, Uberi E.
Georgian Med News. 2014;(237):61-4.
Wilson disease with thrombocytopenia (case report).
11472373
 MIXED_SAMPLE Adult
Haemolytic onset of Wilson disease in a patient with homozygous truncation of ATP7B at Arg1319.
Prella M, Baccala R, Horisberger JD, Belin D, Di Raimondo F, Invernizzi R, Garozzo R, Schapira M.
Br J Haematol. 2001;114(1):230-2.
We describe a 19-year-old woman with haemolytic anaemia and thrombocytopenia as the initial manifestation of Wilson disease (WD).
10604583
 MALE
Albumin dialysis: effective removal of copper in a patient with fulminant Wilson disease and successful bridging to liver transplantation: a new possibility for the elimination of protein-bound toxins.
Kreymann B, Seige M, Schweigart U, Kopp KF, Classen M.
J Hepatol. 1999;31(6):1080-5.
An 18-year-old man with Wilson disease presented with hyperacute liver failure, hepatic encephalopathy III, oligo-anuric renal failure, haemolytic anaemia, rhabdomyolysis, pancreatitis and thrombocytopenia.
3433729
 FEMALE Adult
[New possibilities in the treatment of Wilson-Konovalov disease (hepatolenticular degeneration)].
Kolarski V.
Vutr Boles. 1987;26(5):37-40.
The drug was applied to 3 patients, 18 to 25 years of age, with Wilson-Konovalov disease (hepatolenticular degeneration) who in the course of chronic D-penicillamine treatment developed drug intolerance with signs of nephrotoxicity (in one patient) and myelotoxicity with leucopenia and thrombocytopenia (in two patients).