AMELOGENESIS/DENTINOGENESIS IMPERFECTA: CLINICAL EXOME PANEL (Sec. & CNVs) – 38 genes
LabGenetics
Delivery time
3-4 weeks
Sample
Blood
850,00€
It evaluates inherited enamel and dentin disorders with hypoplasia/hypomaturation, brittle teeth, discoloration, sensitivity, and early tooth loss, both isolated and syndromic (e.g., osteogenesis imperfecta). It allows for precise molecular identification and planning of restoration, prevention, and systemic follow-up. Genes analyzed: AMELX, ENAM, FAM83H, MMP20, KLK4, WDR72, DSPP, COL1A1, COL1A2, LAMB3, and others. You can consult the complete list of analyzed genes by contacting Genotica.
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