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CFP - Properdin deficiency

This test is available for the following conditions:

Conditions > Complement-mediated diseases > Properdin deficiency

This product is also part of the following panels:

Mendelian inherited disorders panel with genome wide CNV analysis
Primary immunodeficiencies panel

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

Method

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

OMIM: 300383
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane

GEN

complete analysis

targeted analysis of a familial mutation

€ 725

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Properdin deficiency

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Gene

CFP - Properdin deficiency

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

Performing laboratory
Radboudumc

€ 725

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CFP - Properdin deficiency

GEN

complete analysis

targeted analysis of a familial mutation

€ 725

Add Update Remove

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