GLA - Fabry disease ¹

This test is available for the following conditions:

  • Conditions > Cardiovascular > Fabry disease

This product is also part of the following panels:

  • Hearing impairment panel (including GJB2)
  • Heart disorders panel¹
  • Hypertrophic cardiomyopathy panel¹
  • Lymphatic anomalies panel with genome wide CNV analysis
  • Mendelian inherited disorders panel with genome wide CNV analysis
  • Metabolic disorders panel
  • Neurological pain disorders panel¹
  • Neuropathies panel¹
  • Painful peripheral neuropathies panel¹
  • Renal disorders panel
  • Skin disorders panel¹

Turnaround time
Complete analysis & Targeted analysis: 4 weeks

Method

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

OMIM: 300644
Performing laboratory: Radboudumc & Maastricht UMC+
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane



€ 369
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Gene

GLA - Fabry disease ¹

Turnaround time
Complete analysis & Targeted analysis: 4 weeks
Performing laboratory
Radboudumc & Maastricht UMC+
€ 369
View Add

GLA - Fabry disease ¹


€ 369
Add