ST3GAL3 - early infantile epileptic encephalopathy type 15

This test is available for the following conditions:

  • Conditions > Intellectual Disability > Early infantile epileptic encephalopathy (EIEE)

This product is also part of the following panels:

  • Comprehensive preconception carrier test panel¹
  • Epilepsy panel
  • Intellectual disability panel with genome wide CNV analysis
  • Mendelian inherited disorders panel with genome wide CNV analysis
  • Metabolic 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: 606494
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 419

Gene

ARHGEF9 - early infantile epileptic encephalopathy type 8

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 410

ARHGEF9 - early infantile epileptic encephalopathy type 8



€ 410

ARHGEF9 - early infantile epileptic encephalopathy type 8

This test is available for the following conditions:

  • Conditions > Intellectual Disability > Early infantile epileptic encephalopathy (EIEE)

This product is also part of the following panels:

  • Epilepsy panel
  • Intellectual disability panel with genome wide CNV analysis
  • Mendelian inherited disorders 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: 300429
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 410
Gene

ARX - early infantile epileptic encephalopathy type 1

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 353

ARX - early infantile epileptic encephalopathy type 1



€ 353

ARX - early infantile epileptic encephalopathy type 1

This test is available for the following conditions:

  • Conditions > Intellectual Disability > Early infantile epileptic encephalopathy (EIEE)

This product is also part of the following panels:

  • Disorders/differences of sex development (DSD) / Primary adrenal insufficiency panel
  • Epilepsy panel
  • Intellectual disability panel with genome wide CNV analysis
  • Mendelian inherited disorders panel with genome wide CNV analysis
  • Movement 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: 308350
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 353
Gene

CACNA1A - early infantile epileptic encephalopathy type 42

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 698

CACNA1A - early infantile epileptic encephalopathy type 42



€ 698

CACNA1A - early infantile epileptic encephalopathy type 42

This test is available for the following conditions:

  • Conditions > Intellectual Disability > Early infantile epileptic encephalopathy (EIEE)

This product is also part of the following panels:

  • Epilepsy panel
  • Intellectual disability panel with genome wide CNV analysis
  • Mendelian inherited disorders panel with genome wide CNV analysis
  • Movement disorders panel
  • Neurological pain disorders panel¹
  • panel spinocerebellar ataxia type 1, 2, 3, 6, 7, 17, DRPLA

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

Method

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

OMIM: 601011
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 698
Gene

CDKL5 - early infantile epileptic encephalopathy type 2

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 764

CDKL5 - early infantile epileptic encephalopathy type 2



€ 764

CDKL5 - early infantile epileptic encephalopathy type 2

This test is available for the following conditions:

  • Conditions > Intellectual Disability > Early infantile epileptic encephalopathy (EIEE)

This product is also part of the following panels:

  • Epilepsy panel
  • Intellectual disability panel with genome wide CNV analysis
  • Mendelian inherited disorders panel with genome wide CNV analysis
  • Mitochondrial disorders panel

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

Method

  • Sequence analysis of all coding exons and flanking intron-exon boundaries
  • Deletion/duplication analysis (MLPA)

OMIM: 300672
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 764
Gene

KCNQ2 - early infantile epileptic encephalopathy type 7

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 452

KCNQ2 - early infantile epileptic encephalopathy type 7



€ 452

KCNQ2 - early infantile epileptic encephalopathy type 7

This test is available for the following conditions:

  • Conditions > Intellectual Disability > Early infantile epileptic encephalopathy (EIEE)

This product is also part of the following panels:

  • Epilepsy panel
  • Intellectual disability panel with genome wide CNV analysis
  • Mendelian inherited disorders 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: 602235
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 452
Gene

KCNT1 - infantile epileptic encephalopathy type 14

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 534

KCNT1 - infantile epileptic encephalopathy type 14



€ 534

KCNT1 - infantile epileptic encephalopathy type 14

This test is available for the following conditions:

  • Conditions > Intellectual Disability > Early infantile epileptic encephalopathy (EIEE)

This product is also part of the following panels:

  • Epilepsy panel
  • Intellectual disability panel with genome wide CNV analysis
  • Mendelian inherited disorders 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: 608167
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 534
Gene

PCDH19 - early infantile epileptic encephalopathy type 9

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 360

PCDH19 - early infantile epileptic encephalopathy type 9



€ 360

PCDH19 - early infantile epileptic encephalopathy type 9

This test is available for the following conditions:

  • Conditions > Intellectual Disability > Early infantile epileptic encephalopathy (EIEE)

This product is also part of the following panels:

  • Epilepsy panel
  • Intellectual disability panel with genome wide CNV analysis
  • Mendelian inherited disorders 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: 300460
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 360
Gene

PLCB1 - early infantile epileptic encephalopathy type 11

Turnaround time
Complete analysis & Targeted analysis: 12 weeks
Performing laboratory
Radboudumc
€ 583

PLCB1 - early infantile epileptic encephalopathy type 11



€ 583

PLCB1 - early infantile epileptic encephalopathy type 11

This test is available for the following conditions:

  • Conditions > Intellectual Disability > Early infantile epileptic encephalopathy (EIEE)

This product is also part of the following panels:

  • Comprehensive preconception carrier test panel¹
  • Epilepsy panel
  • Intellectual disability panel with genome wide CNV analysis
  • Mendelian inherited disorders panel with genome wide CNV analysis
  • Metabolic disorders panel

Turnaround time
Complete analysis & Targeted analysis: 12 weeks

Method

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

OMIM: 607120
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 583
Gene

SCN2A - early infantile epileptic encephalopathy type 11

Turnaround time
Complete analysis & Targeted analysis: 12 weeks
Performing laboratory
Radboudumc
€ 533

SCN2A - early infantile epileptic encephalopathy type 11



€ 533

SCN2A - early infantile epileptic encephalopathy type 11

This test is available for the following conditions:

  • Conditions > Intellectual Disability > Early infantile epileptic encephalopathy (EIEE)

This product is also part of the following panels:

  • Epilepsy panel
  • Intellectual disability panel with genome wide CNV analysis
  • Mendelian inherited disorders panel with genome wide CNV analysis
  • Movement disorders panel

Turnaround time
Complete analysis & Targeted analysis: 12 weeks

Method

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

OMIM: 182390
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 533
Gene

SCN8A - early infantile epileptic encephalopathy type 13

Turnaround time
Complete analysis & Targeted analysis: 12 weeks
Performing laboratory
Radboudumc
€ 473

SCN8A - early infantile epileptic encephalopathy type 13



€ 473

SCN8A - early infantile epileptic encephalopathy type 13

This test is available for the following conditions:

  • Conditions > Intellectual Disability > Early infantile epileptic encephalopathy (EIEE)

This product is also part of the following panels:

  • Epilepsy panel
  • Intellectual disability panel with genome wide CNV analysis
  • Mendelian inherited disorders panel with genome wide CNV analysis
  • Movement disorders panel
  • Neurological pain disorders panel¹
  • Painful peripheral neuropathies panel¹

Turnaround time
Complete analysis & Targeted analysis: 12 weeks

Method

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

OMIM: 600702
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 473
Gene

SLC25A22 - early infantile epileptic encephalopathy type 3

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 369

SLC25A22 - early infantile epileptic encephalopathy type 3



€ 369

SLC25A22 - early infantile epileptic encephalopathy type 3

This test is available for the following conditions:

  • Conditions > Intellectual Disability > Early infantile epileptic encephalopathy (EIEE)

This product is also part of the following panels:

  • Comprehensive preconception carrier test panel¹
  • Epilepsy panel
  • Intellectual disability panel with genome wide CNV analysis
  • Mendelian inherited disorders panel with genome wide CNV analysis
  • Mitochondrial 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: 609302
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 369
Gene

SPTAN1 - early infantile epileptic encephalopathy type 5

Turnaround time
12 weeks
Performing laboratory
Radboudumc
€ 657

SPTAN1 - early infantile epileptic encephalopathy type 5



€ 657

SPTAN1 - early infantile epileptic encephalopathy type 5

This test is available for the following conditions:

  • Conditions > Intellectual Disability > Early infantile epileptic encephalopathy (EIEE)

This product is also part of the following panels:

  • Epilepsy panel
  • Intellectual disability panel with genome wide CNV analysis
  • Mendelian inherited disorders panel with genome wide CNV analysis
  • Movement disorders panel
  • Neuropathies panel¹

Turnaround time
12 weeks

Method

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

OMIM: 182810
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 657
Gene

ST3GAL3 - early infantile epileptic encephalopathy type 15

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 419

ST3GAL3 - early infantile epileptic encephalopathy type 15



€ 419
Gene

STXBP1 - early infantile epileptic encephalopathy type 4

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 468

STXBP1 - early infantile epileptic encephalopathy type 4



€ 468

STXBP1 - early infantile epileptic encephalopathy type 4

This test is available for the following conditions:

  • Conditions > Intellectual Disability > Early infantile epileptic encephalopathy (EIEE)

This product is also part of the following panels:

  • Epilepsy panel
  • Intellectual disability panel with genome wide CNV analysis
  • Mendelian inherited disorders panel with genome wide CNV analysis
  • Mitochondrial 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: 602926
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 468
Gene

TBC1D24 - early infantile epileptic encephalopathy type 16

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 377

TBC1D24 - early infantile epileptic encephalopathy type 16



€ 377

TBC1D24 - early infantile epileptic encephalopathy type 16

This test is available for the following conditions:

  • Conditions > Intellectual Disability > Early infantile epileptic encephalopathy (EIEE)

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
  • Skin disorders panel¹

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

Method

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

OMIM: 615338
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 377