KLHL3 - pseudohypoaldosteronism type IID
This test is available for the following conditions:
- Conditions > Endocrine > Pseudohypoaldosteronism
- Conditions > Renal / Nephrological > Pseudohypoaldosteronism
This product is also part of the following panels:
- Comprehensive preconception carrier test 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:
605775
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane
WNK4 - pseudohypoaldosteronism type IIB
This test is available for the following conditions:
- Conditions > Endocrine > Pseudohypoaldosteronism
- Conditions > Renal / Nephrological > Pseudohypoaldosteronism
This product is also part of the following panels:
- 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:
601844
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane