KCNQ1 - Jervell and Lange-Nielsen syndrome

This test is available for the following conditions:

  • Conditions > Cardiovascular > Jervell and Lange-Nielsen syndrome
  • Conditions > Hearing impairment > Jervell and Lange-Nielsen syndrome

This product is also part of the following panels:

  • Arrhythmia and cardiac conduction disorders panel¹
  • Comprehensive preconception carrier test panel¹
  • Hearing impairment panel (including GJB2)
  • Heart disorders panel¹
  • Long QT syndrome panel¹
  • Mendelian inherited disorders panel with genome wide CNV analysis
  • panel Jervell and Lange-Nielsen syndrome (KCNQ1, KCNE1) ¹

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

Method

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

OMIM: 607542
Performing laboratory: Maastricht UMC+
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 476

Panel

panel Jervell and Lange-Nielsen syndrome (KCNQ1, KCNE1) ¹

Turnaround time
8 weeks
Performing laboratory
Maastricht UMC+
€ 527

panel Jervell and Lange-Nielsen syndrome (KCNQ1, KCNE1) ¹



€ 527

panel Jervell and Lange-Nielsen syndrome (KCNQ1, KCNE1) ¹

This test is available for the following conditions:

  • Conditions > Cardiovascular > Jervell and Lange-Nielsen syndrome
  • Conditions > Hearing impairment > Jervell and Lange-Nielsen syndrome

Turnaround time
8 weeks

Method

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

Performing laboratory: Maastricht UMC+
Authorized material(s): EDTA blood, Isolated DNA




€ 527
Gene

KCNE1 - Jervell and Lange-Nielsen syndrome type 2 ¹

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Maastricht UMC+
€ 336

KCNE1 - Jervell and Lange-Nielsen syndrome type 2 ¹



€ 336

KCNE1 - Jervell and Lange-Nielsen syndrome type 2 ¹

This test is available for the following conditions:

  • Conditions > Cardiovascular > Jervell and Lange-Nielsen syndrome
  • Conditions > Hearing impairment > Jervell and Lange-Nielsen syndrome

This product is also part of the following panels:

  • Arrhythmia and cardiac conduction disorders panel¹
  • Comprehensive preconception carrier test panel¹
  • Hearing impairment panel (including GJB2)
  • Heart disorders panel¹
  • Long QT syndrome panel¹
  • Mendelian inherited disorders panel with genome wide CNV analysis
  • panel Jervell and Lange-Nielsen syndrome (KCNQ1, KCNE1) ¹

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

Method

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

OMIM: 176261
Performing laboratory: Maastricht UMC+
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 336
Gene

KCNQ1 - Jervell and Lange-Nielsen syndrome

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Maastricht UMC+
€ 476

KCNQ1 - Jervell and Lange-Nielsen syndrome



€ 476