PDHX - Lacticacidemia due to PDX1 deficiency

This test is available for the following conditions:

  • Conditions > Mitochondrial disorders > Pyruvate dehydrogenase deficiency

This product is also part of the following panels:

  • Comprehensive preconception carrier test panel¹
  • Epilepsy panel
  • Intellectual disability panel
  • Mendelian inherited disorders panel
  • Mitochondrial disorders panel
  • 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: 608769
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 725

Gene

DLAT - Pyruvate dehydrogenase deficiency

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 725

DLAT - Pyruvate dehydrogenase deficiency



€ 725

DLAT - Pyruvate dehydrogenase deficiency

This test is available for the following conditions:

  • Conditions > Mitochondrial disorders > Pyruvate dehydrogenase deficiency

This product is also part of the following panels:

  • Comprehensive preconception carrier test panel¹
  • Epilepsy panel
  • Intellectual disability panel
  • Mendelian inherited disorders panel
  • Mitochondrial disorders panel
  • 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: 608770
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 725
Gene

PDHA1 - Pyruvate dehydrogenase deficiency

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 725

PDHA1 - Pyruvate dehydrogenase deficiency



€ 725

PDHA1 - Pyruvate dehydrogenase deficiency

This test is available for the following conditions:

  • Conditions > Mitochondrial disorders > Pyruvate dehydrogenase deficiency

This product is also part of the following panels:

  • Epilepsy panel
  • Intellectual disability panel
  • Mendelian inherited disorders panel
  • Mitochondrial disorders panel
  • Movement disorders panel
  • Neuropathies panel¹

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

Method

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

OMIM: 300502
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 725
Gene

PDHB - Pyruvate dehydrogenase deficiency

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 725

PDHB - Pyruvate dehydrogenase deficiency



€ 725

PDHB - Pyruvate dehydrogenase deficiency

This test is available for the following conditions:

  • Conditions > Mitochondrial disorders > Pyruvate dehydrogenase deficiency

This product is also part of the following panels:

  • Comprehensive preconception carrier test panel¹
  • Epilepsy panel
  • Intellectual disability panel
  • Mendelian inherited disorders panel
  • 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: 179060
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 725
Gene

PDHX - Lacticacidemia due to PDX1 deficiency

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 725

PDHX - Lacticacidemia due to PDX1 deficiency



€ 725