CYP17A1 - isolated 17,20-lyase deficiency

This test is available for the following conditions:

  • Conditions > Disorders in sex development > 17,20-lyase deficiency, isolated

This product is also part of the following panels:

  • WES comprehensive preconception carrier test ¹
  • WES disorders of sex development (99.6% **)
  • WES Mendelian inherited disorders (99.6% **)
  • WES metabolic disorders (99.6% **)

** % of the coding region of this gene has a coverage of >20x. (Without % information : This is a non-coding gene for which coverage statistics could not be determined)

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

Method

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

OMIM: 609300
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 377

Gene

CYP17A1 - isolated 17,20-lyase deficiency

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

CYP17A1 - isolated 17,20-lyase deficiency



€ 377