Periodic Paralysis Panel
Clinical Genetic Test
Help
offered by
GTR Test Accession: Help GTR000592445.1
METABOLIC DISEASENERVOUS SYSTEMINHERITED DISEASE ... View more
Last updated in GTR: 2021-02-25
Last annual review date for the lab: 2024-03-25 LinkOut
At a Glance
Diagnosis
Andersen Tawil syndrome; Hypokalemic periodic paralysis, type 1; Hypokalemic periodic paralysis, type 2
Genes (9): Help
ATP1A2 (1q23.2), CACNA1S (1q32.1), CLCN1 (7q34), KCNJ2 (17q24.3), KCNJ5 (11q24.3), ...
Molecular Genetics - Deletion/duplication analysis: Next-Generation (NGS)/Massively parallel sequencing (MPS); ...
Not provided
Not provided
Not provided
Ordering Information
Test Order Code: Help
TG81
Informed consent required: Help
Decline to answer
Pre-test genetic counseling required: Help
Decline to answer
Post-test genetic counseling required: Help
Decline to answer
Recommended fields not provided:
Conditions Help
Total conditions: 3
Condition/Phenotype Identifier
Test Targets
Genes Help
Total genes: 9
Gene Associated Condition Germline or Somatic Allele (Lab-provided) Variant in NCBI
Methodology
Total methods: 2
Method Category Help
Test method Help
Instrument *
Deletion/duplication analysis
Next-Generation (NGS)/Massively parallel sequencing (MPS)
Sequence analysis of the entire coding region
Next-Generation (NGS)/Massively parallel sequencing (MPS)
* Instrument: Not provided
Clinical Information
Test purpose: Help
Diagnosis
Recommended fields not provided:
Technical Information
Availability: Help
Tests performed
Entire test performed in-house
Analytical Validity: Help
Based on analytical validation studies, Next Generation Sequencing (NGS) has a sensitivity of >99% for identifying single nucleotide variants (SNV).
Proficiency testing (PT):
Is proficiency testing performed for this test? Help
No
Recommended fields not provided:
Regulatory Approval
FDA Review: Help
Not provided
Additional Information

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