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Management of hepatolenticular degeneration during pregnancy / 中华肝脏病杂志
Chinese Journal of Hepatology ; (12): 107-109, 2022.
Article de Zh | WPRIM | ID: wpr-935918
Bibliothèque responsable: WPRO
ABSTRACT
Hepatolenticular degeneration (Wilson's disease, WD) is a kind of autosomal recessive genetic disease characterized by disorders of copper metabolism. It is caused by mutations in the ATP7B gene, resulting in impaired excretion of copper into the bile, and then pathological deposition in the liver, brain, and other organs. Early diagnosis and treatment can significantly improve the prognosis of patients with WD. However, there is still no clear consensus on the treatment and management of WD during pregnancy. Herein, the clinical management of WD during pregnancy is summarized for clinicians' reference.
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Texte intégral: 1 Indice: WPRIM Sujet Principal: Cuivre / Copper-transporting ATPases / Dégénérescence hépatolenticulaire / Mutation Type d'étude: Screening_studies Limites du sujet: Female / Humans / Pregnancy langue: Zh Texte intégral: Chinese Journal of Hepatology Année: 2022 Type: Article
Texte intégral: 1 Indice: WPRIM Sujet Principal: Cuivre / Copper-transporting ATPases / Dégénérescence hépatolenticulaire / Mutation Type d'étude: Screening_studies Limites du sujet: Female / Humans / Pregnancy langue: Zh Texte intégral: Chinese Journal of Hepatology Année: 2022 Type: Article