Witkop syndrome

MSX1 - Witkop syndrome ¹

This test is available for the following conditions:

• Conditions > Skin > Witkop syndrome

This product is also part of the following panels:

• Craniofacial anomalies panel with genome wide CNV analysis
• Mendelian inherited disorders panel with genome wide CNV analysis
• Orofacial clefting panel with genome wide CNV analysis
• panel oligodontie (WNT10A, MSX1, PAX9, AXIN2) ¹
• 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

OMIM: 142983
Performing laboratory: Maastricht UMC+
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane

---