GENETIC DIAGNOSTICS AND CLINICAL FEATURES OF WILSON’S DISEASE IN CHILDREN

GENETIC DIAGNOSTICS AND CLINICAL FEATURES OF WILSON’S DISEASE IN CHILDREN

A disorder of copper metabolism at Wilson’s disease (WD), conditioned by a mutation of adenosine thriphospate P-type gene (ATP7B), results in irreversible changes in the liver and in the nervous system. Mortality is high at WD, but it is one of hereditary diseases, well subjected to the therapy. The...

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Bibliographic Details
Main Authors: Ivanna Haiboniuk, Marta Dats-Opoka, Halyna Makukh, Yaryna Boyko, Igor Kiselyk
Format: Article
Language:English
Published: Scientific Route OÜ 2020-03-01
Series:EUREKA: Life Sciences
Subjects:
wilson’s disease
hepatobiliary disorders
children
genetic testing
mutation of atp7b gene
Online Access:http://eu-jr.eu/life/article/view/1197/1178

Internet

http://eu-jr.eu/life/article/view/1197/1178

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