Anderson syndrome

KCNJ2 - Andersen syndrome¹

This test is available for the following conditions:

• Conditions > Cardiovascular > Anderson syndrome

This product is also part of the following panels:

• Arrhythmia and cardiac conduction disorders panel¹
• Heart disorders panel¹
• Long QT syndrome panel¹
• Mendelian inherited disorders panel with genome wide CNV analysis
• Muscle disorders panel
• Orofacial clefting panel with genome wide CNV analysis
• Short stature/skeletal dysplasia panel with genome wide CNV analysis

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

Method

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

OMIM: 600681
Performing laboratory: Maastricht UMC+
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane

---