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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
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
