FOXL2 - blepharophimosis, epicanthus inversus, and ptosis

This test is available for the following conditions:

  • Conditions > Multiple congenital anomalies (MCA) > Blepharophimosis, epicantus inversus and ptosis

This product is also part of the following panels:

  • Disorders/differences of sex development (DSD) / Primary adrenal insufficiency panel
  • Mendelian inherited disorders panel with genome wide CNV analysis
  • Premature ovarian insufficiency panel

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

Method

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

OMIM: 110100
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 327

Gene

FOXL2 - blepharophimosis, epicanthus inversus, and ptosis

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 327

FOXL2 - blepharophimosis, epicanthus inversus, and ptosis



€ 327