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.

Abdominal pain

An unpleasant sensation characterized by physical discomfort (such as pricking, throbbing, or aching) and perceived to originate in the abdomen.


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(per page)
PMID (PMCID)
24349711
(3863963)
 OTHER
Wandering spleen with gastric volvulus and intestinal non-rotation in an adult male patient.
Ooka M, Kohda E, Iizuka Y, Nagamoto M, Ishii T, Saida Y, Shimizu N, Gomi T.
Acta Radiol Short Rep. 2013;2(7):2047981613499755.
A 22-year-old man who had been previously treated for Wilson disease was admitted with severe abdominal pain.
12211729
 FEMALE Adult
Acute haemolytic syndrome and liver failure as the first manifestations of Wilson's disease.
Dabrowska E, Jablonska-Kaszewska I, Ozieblowski A, Falkiewicz B.
Med Sci Monit. 2001;7 Suppl 1:246-51.
Acute liver failure and haemolytic syndrome appeared quite suddenly as the first manifestations of Wilson disease (WD) in five of our patients previously regarded as healthy persons (although an interview showed that 2-4 weeks prior to the illness the patients complained of several non-specific symptoms, such as abdominal pain, headaches, fever, weakness or behavioural changes).