Advance in the pathogenesis and treatment of Wilson disease
<p>Abstract</p> <p>Wilson disease is an autosomal recessive disorder of copper metabolism. Diagnosis depends primarily on clinical features, biochemical parameters and the presence of the Kayser-Fleischer ring. Genetic analysis for mutations within <it>ATP7B</it> is a c...
Main Authors: | Dong Qin-Yun, Wu Zhi-Ying |
---|---|
Format: | Article |
Language: | English |
Published: |
BMC
2012-11-01
|
Series: | Translational Neurodegeneration |
Subjects: | |
Online Access: | http://www.translationalneurodegeneration.com/content/1/1/23 |
Similar Items
-
Advances in Treatment of Wilson Disease
by: Annu Aggarwal, et al.
Published: (2018-02-01) -
MODERN ASPECTS OF PATHOGENETIC TREATMENT WITH ZINC SALTS OF PATIENTS WITH WILSON'S DISEASE IN UKRAINE
by: Ivan Voloshyn-Gaponov
Published: (2019-12-01) -
Ammonium tetrathiomolybdate in the decoppering phase treatment of Wilson's disease with neurological symptoms: A case series
by: Oriol De Fabregues, et al.
Published: (2020-05-01) -
Regulation of murine copper homeostasis by members of the COMMD protein family
by: Amika Singla, et al.
Published: (2021-01-01) -
Nephrotic syndrome after treatment with D-penicillamine in a patient with Wilson’s disease
by: Kostadinova Anna D., et al.
Published: (2014-06-01)