CYP19A1 - aromatase deficiency
This test is available for the following conditions:
- Conditions > Disorders in sex development > Aromatese deficiency
This product is also part of the following panels:
- Comprehensive preconception carrier test panel¹
- Disorders/differences of sex development (DSD) / Primary adrenal insufficiency panel
- Mendelian inherited disorders panel with genome wide CNV analysis
- Metabolic disorders panel
- Premature ovarian insufficiency panel
- Tall stature panel with genome wide CNV analysis
                Turnaround time
                Complete analysis: 8 weeks / Targeted analysis: 4 weeks
            
Method
- Sequence analysis of all coding exons and flanking intron-exon boundaries
                    OMIM: 
107910                    
                    Performing laboratory: Radboudumc
                    Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane
            
