Athena Diagnostics - Testing that Makes a Difference
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Lamin A/C DNA Sequencing Test #565
Type of Disorder: Neuromuscular Disorders
Typical Presentation: LMNA mutations have been associated with a variety of clinical syndromes including limb girdle muscular dystrophy (most common), Charcot-Marie-Tooth disease., dilated cardiomyopathy, Emery-Dreifuss muscular dystrophy, lipodystrophy disorders
Indications for Testing: See Typical Presentation. Also, family members of patients with previously identified LMNA mutations.
Disease(s) tested for: Limb girdle muscular dystrophy, Emery-Dreifuss Muscular Dystrophy
Test Details
Test Code: 565
Profiles that contain this test: Emery-Dreifuss Muscular Dystrophy Evaluation
Informed Consent Required: Yes
Medicare ABN Required: Yes
Technical Information
Utility: Detects sequence variations in the <i>LMNA<i> gene
Methodology: PCR and DNA sequencing
Reference Value: No sequence variations detected
CPT Coding
The CPT codes provided are based on AMA guidelines and are for informational purposes only. CPT coding is the sole responsibility of the billing party. Please direct any questions regarding coding to the payer being billed.
Stacked CPT Code(s): 83891(1), 83898(11), 83904(11), 83909(11), 83912(1)
Shipping Considerations
Please label each specimen tube with two forms of patient identification. These forms of identification must also appear on the requisition form.
Preferred Specimen Requirements
Type: Whole blood
Minimum Volume: 15ml
Collection Tube: Lavender top (EDTA)
Storage Conditions: Must be refrigerated
Shipping Conditions: Ship at room temperature or on ice pack. Ship Monday - Thursday only.
Test Turnaround: 4 - 6 weeks
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