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
  • Mendelian inherited disorders panel
  • 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



€ 345
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Gene

KCNJ10 - SESAME syndrome

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 345
View Add

KCNJ10 - SESAME syndrome


€ 345
Add