SCNN1B - Liddle syndrome

This test is available for the following conditions:

  • Conditions > Endocrine > Liddle syndrome
  • Conditions > Renal / Nephrological > Liddle syndrome

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 selected exons and flanking intron-exon boundaries
Remarks
Liddle syndrome can be caused by activating mutations in the last exon of the SCNN1B gene. Therefore only this exon is analyzed.

OMIM: 600760
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 320

Gene

SCNN1B - Liddle syndrome

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 320

SCNN1B - Liddle syndrome



€ 320
Gene

SCNN1G - Liddle syndrome

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 320

SCNN1G - Liddle syndrome



€ 320

SCNN1G - Liddle syndrome

This test is available for the following conditions:

  • Conditions > Endocrine > Liddle syndrome
  • Conditions > Renal / Nephrological > Liddle syndrome

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 selected exons and flanking intron-exon boundaries
Remarks
Liddle syndrome can be caused by activating mutations in the last exon of the SCNN1G gene. Therefore only this exon is analyzed.

OMIM: 600761
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 320