SeSAME syndrome

KCNJ10 - SESAME syndrome

This test is available for the following conditions:

• Conditions > Multiple congenital anomalies (MCA) > SeSAME syndrome
• Conditions > Hearing impairment > SeSAME syndrome
• Conditions > Renal / Nephrological > SeSAME syndrome
• Conditions > Neurological > SeSAME syndrome

This product is also part of the following panels:

• Comprehensive preconception carrier test panel¹
• Epilepsy panel
• Hearing impairment panel (including GJB2)
• Intellectual disability panel with genome wide CNV analysis
• Mendelian inherited disorders panel with genome wide CNV analysis
• Movement disorders panel
• 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: 602208
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane

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