Wilson's disease - case study

被引：0

作者：

Adamczak-Ratajczak, Agnieszka ^{[1
]}

Krawczyk, Mieczyslaw ^{[2
]}

Zywert, Marek ^{[2
]}

Wronka, Jaroslaw ^{[2
]}

Gibas, Magdalena ^{[1
]}

Madry, Edyta ^{[1
]}

机构：

[1] Uniwersytetu Medycznego Poznaniu, Katedra Zaklad Fizjol, Poznan, Poland

[2] NZOZ Centrum Medyczne HCP Poznaniu, Oddzial Neurol, Poznan, Poland

来源：

FAMILY MEDICINE AND PRIMARY CARE REVIEW | 2009年 / 11卷 / 03期

关键词：

Wilson's disease; pathogenesis; diagnosis; treatment;

D O I：

暂无

中图分类号：

R1 [预防医学、卫生学];

学科分类号：

1004 ; 120402 ;

摘要：

Wilson's disease is rare genetic autosomal recessive disorder. It is characterized by excessive copper deposits, mainly in parenchymal organs, leading to their damage. Studies in Europe have estimated the prevelence rate to be 30-90 cases per million population. Untreated Wilson's disease has progressive, irreversible consequences, and ultimately causes death.

引用

页码：808 / 811

页数：4