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Test ID: FFDMC
Complete DMD Evaluation - Females

Secondary ID A test code used for billing and in test definitions created prior to November 2011

91581

NY State Approved Indicates the status of NY State approval and if the test is orderable for NY State clients.

Yes

Profile Information A profile is a group of laboratory tests that are ordered and performed together under a single Mayo Test ID. Profile information lists the test performed, inclusive of the test fee, when a profile is ordered and includes reporting names and individual availability.

Test IDReporting NameAvailable SeparatelyAlways Performed
FPDMFPartial DMD Del/DupNoYes
FPDMSPartial DMD SequencingNoNo

Testing Algorithm Delineates situation(s) when tests are added to the initial order. This includes reflex and additional tests.

DMD Deletion/Duplication is performed first. If no mutations are

found in the first analysis, or if the mutations cannot be confirmed,

sequence analysis of all 79 exons will be performed.

Method Name A short description of the method used to perform the test

DMD Deletion/duplication:

Dosage analysis of all exons on the DMD gene.

 

DMD Sequencing:

PCR and DNA Sequencing

Reporting Name A shorter/abbreviated version of the Published Name for a test; an abbreviated test name

Complete DMD Evaluation-Females

Aliases Lists additional common names for a test, as an aid in searching

DMD/BMD
Duchenne Muscular Dystrophy
Duchenne/Becker Muscular Dystrophy

Specimen Type Describes the specimen type needed for testing

Whole Blood EDTA

Specimen Required Defines the optimal specimen. This field describes the type of specimen required to perform the test and the preferred volume to complete testing. The volume allows automated processing, fastest throughput and, when indicated, repeat or reflex testing.

40 mL whole blood collected in a lavender top EDTA tube.

Send whole blood at ambient temperature.

 

Note:  Collection date is required.

Specimen Minimum Volume Defines the amount of specimen required to perform an assay once, including instrument and container dead space. Submitting the minimum specimen volume makes it impossible to repeat the test or perform confirmatory or perform reflex testing. In some situations, a minimum specimen volume may result in a QNS (quantity not sufficient) result, requiring a second specimen to be collected.

20 mL

Reject Due To Identifies specimen types and conditions that may cause the specimen to be rejected

Specimens other than

Whole blood

Anticoagulants other than

EDTA

Hemolysis

NA

Thawing

NA

Lipemia

NA

Icteric

NA

Specimen Stability Information Provides a description of the temperatures required to transport a specimen to the laboratory. Alternate acceptable temperature(s) are also included.

Specimen TypeTemperatureTime
Whole Blood EDTAAmbient (preferred)72 hours
 Refrigerated 72 hours

Reference Values Describes reference intervals and additional information for interpretation of test results. May include intervals based on age and sex when appropriate. Intervals are Mayo-derived, unless otherwise designated. If an interpretive report is provided, the reference value field will state this.

An interpretive report will be faxed and/or mailed under separate cover.

 

Test Performed by:  Athena Diagnostics

                              377 Plantation St

                              Four Biotech Park

                              Worcester, MA 01605

Day(s) and Time(s) Test Performed Outlines the days and times the test is performed. This field reflects the day and time the sample must be in the testing laboratory to begin the testing process and includes any specimen preparation and processing time required before the test is performed. Some tests are listed as continuously performed, which means assays are performed several times during the day.

Monday, Thursday

Analytic Time Defines the amount of time it takes the laboratory to setup and perform the test. This is defined in number of days. The shortest interval of time expressed is "same day/1 day," which means the results may be available the same day that the sample is received in the testing laboratory. One day means results are available 1 day after the sample is received in the laboratory.

6 - 8 weeks

Maximum Laboratory Time Defines the maximum time from specimen receipt at Mayo Medical Laboratories until the release of the test result

6 - 8 weeks

Performing Laboratory Location The location of the laboratory that performs the test

Athena Diagnostics

CPT Code Information Provides guidance in determining the appropriate Current Procedural Terminology (CPT) code(s) information for each test or profile. The listed CPT codes reflect Mayo Medical Laboratories interpretation of CPT coding requirements. It is the responsibility of each laboratory to determine correct CPT codes to use for billing.

81161

81408

LOINC® Code Information Provides guidance in determining the Logical Observation Identifiers Names and Codes (LOINC) values for the result codes returned for this test or profile.

Result IDReporting NameLOINC Code
Z0091Partial DMD Del/DupIn Process
Z0092Partial DMD SequencingIn Process