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Journal of Zhejiang University. Medical sciences ; (6): 612-618, 2014.
Article Dans Chinois | WPRIM | ID: wpr-251655

Résumé

It has been proven that familial aldosteronism type I is related to 11-beta hydroxylase (CYP11B1)/aldosterone synthase (CYP11B2) chimeric genes. In recent years, accumulated evidences indicate that the genetic basis of primary aldosteronism may involve chromosome 7p22 candidate genes, polymorphisms of CYP11B1 and CYP11B2 genes, mutations of ion channel- related KCNJ5, ATP1A1, CACNA1D genes. The article reviews the progress on genetic basis of primary aldosteronism.


Sujets)
Humains , Cytochrome P-450 CYP11B2 , Génétique , Hyperaldostéronisme , Génétique , Mutation , Polymorphisme génétique , Steroid 11-beta-hydroxylase , Génétique
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