Ophthalmoplegia, chronic progressive (PEO)

DNA2 - Progressive external ophthalmoplegia with mitochondrial DNA deletions

This test is available for the following conditions:

• Conditions > Mitochondrial disorders > Ophthalmoplegia, chronic progressive (PEO)

This product is also part of the following panels:

• Comprehensive preconception carrier test panel¹
• Mendelian inherited disorders panel with genome wide CNV analysis
• Mitochondrial disorders panel
• Muscle disorders panel
• Short stature/skeletal dysplasia 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

Remarks
We prefer DNA from muscle tissue.

OMIM: 601810
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane

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