CTDP1 (c.863+389C>T) - congenital cataracts with facial dysmorphism and neuropathy

This test is available for the following conditions:

  • Conditions > Multiple congenital anomalies (MCA) > Congenital cataracts with facial dysmorphism and neuropathy
  • Conditions > Vision impairment / blindness > Congenital cataracts with facial dysmorphism and neuropathy

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

Method

  • Sequence analysis of all coding exons and flanking intron-exon boundaries
Remarks
Targetted mutation analysis of the only known pathogenic mutation (c.863+389C>T) in this gene.

OMIM: 604168
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane



€ 320
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Gene

CTDP1 (c.863+389C>T) - congenital cataracts with facial dysmorphism and neuropathy

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 320
View Add

CTDP1 (c.863+389C>T) - congenital cataracts with facial dysmorphism and neuropathy


€ 320
Add