Hyperaldosteronism, familial

KCNJ5 - familial hyperaldosteronism type 3

This test is available for the following conditions:

• Conditions > Endocrine > Hyperaldosteronism, familial

This product is also part of the following panels:

• Heart disorders panel¹
• Mendelian inherited disorders panel with genome wide CNV analysis
• Renal disorders panel

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks

Method

• Sequence analysis of all coding exons and flanking intron-exon boundaries

OMIM: 600734
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane

---