CYP1B1 - autosomal recessive primary congenital glaucoma type 3A

This test is available for the following conditions:

  • Conditions > Vision impairment / blindness > Glaucoma

This product is also part of the following panels:

  • Comprehensive preconception carrier test panel¹
  • Mendelian inherited disorders panel with genome wide CNV analysis
  • Metabolic disorders panel
  • Vision 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: 601771
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 336

Gene

CYP1B1 - autosomal recessive primary congenital glaucoma type 3A

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 336

CYP1B1 - autosomal recessive primary congenital glaucoma type 3A



€ 336
Gene

LTBP2 - primary congenital glaucoma type 3D

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 583

LTBP2 - primary congenital glaucoma type 3D



€ 583

LTBP2 - primary congenital glaucoma type 3D

This test is available for the following conditions:

  • Conditions > Vision impairment / blindness > Glaucoma

This product is also part of the following panels:

  • Comprehensive preconception carrier test panel¹
  • Mendelian inherited disorders panel with genome wide CNV analysis
  • Short stature/skeletal dysplasia panel with genome wide CNV analysis
  • Vision 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: 602091
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 583