Lymphedema-distichiasis syndrome

FOXC2 - lymphedema-distichiasis syndrome ¹

This test is available for the following conditions:

• Conditions > Skin > Lymphedema-distichiasis syndrome

This product is also part of the following panels:

• Heart disorders panel¹
• Lymphatic anomalies panel with genome wide CNV analysis
• Mendelian inherited disorders panel with genome wide CNV analysis
• Orofacial clefting panel with genome wide CNV analysis
• Renal disorders panel
• Skin disorders panel¹

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)

OMIM: 602402
Performing laboratory: Maastricht UMC+
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane

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