NDP - Norrie disease
This test is available for the following conditions:
- Conditions > Intellectual Disability > Norrie disease
 - Conditions > Multiple congenital anomalies (MCA) > Norrie disease
 - Conditions > Vision impairment / blindness > Norrie disease
 
This product is also part of the following panels:
- Hearing impairment panel (including GJB2)
 - Intellectual disability / developmental delay panel with genome wide CNV analysis
 - Mendelian inherited disorders 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
 - Deletion/duplication analysis (MLPA)
 
MLPA analysis only if patient is a woman.
                    OMIM: 
300658                    
                    Performing laboratory: Radboudumc
                    Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane