EMD Sequencing
GTR Test Accession: Help GTR000500918.1
INHERITED DISEASECARDIOVASCULARMUSCULOSKELETAL ... View more
Registered in GTR: 2013-04-02
Last annual review date for the lab: 2024-07-01 LinkOut
At a Glance
Diagnosis
Emery-Dreifuss muscular dystrophy
Genes (1): Help
EMD (Xq28)
Molecular Genetics - Mutation scanning of the entire coding region: Bi-directional Sanger Sequence Analysis
Individuals with suspected Emery-Dreifuss Muscular Dystrophy
Not provided
Not provided
Ordering Information
Offered by: Help
Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory
View lab's website
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: 1
Condition/Phenotype Identifier
Test Targets
Genes Help
Total genes: 1
Gene Associated Condition Germline or Somatic Allele (Lab-provided) Variant in NCBI
Methodology
Total methods: 1
Method Category Help
Test method Help
Instrument *
Mutation scanning of the entire coding region
Bi-directional Sanger Sequence Analysis
* Instrument: Not provided
Clinical Information
Test purpose: Help
Diagnosis
Target population: Help
Individuals with suspected Emery-Dreifuss Muscular Dystrophy
Recommended fields not provided:
Technical Information
Availability: Help
Tests performed
Entire test performed in-house
Analytical Validity: Help
This test detects over 99% of substitution variants and small insertions and deletions
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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