Alkaline Phosphatase Panel
Alkaline Phosphatase Panel
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The Alkaline Phosphatase panel is a genetic test used to identify mutations in the ALPL gene, which is involved in bone mineralization and metabolism. Mutations in this gene can lead to hypophosphatasia, a rare genetic disorder characterized by defective bone and teeth mineralization. The panel tests for genetic variants that are known to affect these processes.
This panel is designed for individuals with a family history of hypophosphatasia or individuals with symptoms of the condition, such as skeletal abnormalities, dental problems, and muscle weakness. Genetic testing can confirm a diagnosis, inform treatment and management decisions, and guide family planning. Testing can also provide reassurance for unaffected family members.
The analysis takes into consideration the mutation of germline DNA, it investigates SNP and Indel mutations up to 150 bp.
- Available in less than 24 hours
- Based on Whole Genome Sequencing
- 3 or more genes analyzed
- Investigates SNP and Indel mutations up to 150 bp
List of main conditions:
- Alkaline Phosphatase

Dieses Produkt ist nur für Kunden gedacht, die bereits einen MyGenome-Test erworben haben.