Aconitase deficiency

ACO2 - Mitochondrial aconitase deficiency - Infantile cerebellar-retinal degeneration

This test is available for the following conditions:

• Conditions > Mitochondrial disorders > Aconitase deficiency

This product is also part of the following panels:

• Comprehensive preconception carrier test panel¹
• Epilepsy panel
• Intellectual disability panel
• Mendelian inherited disorders panel
• Metabolic disorders panel
• Mitochondrial disorders panel
• Movement disorders panel
• 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

OMIM: 100850
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane

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