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.

Ecchymosis

A purpuric lesion that is larger than 1 cm in diameter.


Total: 1

                       


(per page)
PMID (PMCID)
27639912
 FEMALE
[Ecchymosis as the presenting manifestation of Wilson disease: A case report].
Bayer G, Bauvois A, Mankikian J, Tardieu M, Maillot F, Salame E, Woimant F, Poujois A, Viana M, Legras A.
Rev Med Interne. 2017;38(6):416-419.
[Ecchymosis as the presenting manifestation of Wilson disease: A case report].