Periodic Paralysis Panel
Periodic Paralysis Panel
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Pendred syndrome is a genetic disorder that causes early hearing loss in children. It can also affect the thyroid gland and sometimes create balance problems. The syndrome is named after Vaughan Pendred, the physician who first described people with the disorder.
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
- More than 85 genes analyzed
- Investigates SNP and Indel mutations up to 150 bp
List of main conditions:
- Hypokalemic Periodic Paralysis

Questo prodotto è destinato esclusivamente ai clienti che hanno già acquistato un test MyGenome