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Test Code ACMFSM Acetylcholine Receptor Modulating Antibody, Flow Cytometry Assay, Serum

Additional Codes

Mayo ACMFS
Epic ID LAB3316

 

Specimen Type

Serum


Ordering Guidance


Typically, physicians will order acetylcholine receptor (AChR) binding, blocking, and modulating antibodies. Mayo Clinic Laboratories' (MCL) tests are not named in that manner; instead these are offered as myasthenia gravis (MG) evaluations. MGMR / Myasthenia Gravis Evaluation with Muscle-Specific Kinase (MuSK) Reflex, Serum is the testing of choice in most cases.

 

AChR blocking antibody testing is no longer offered individually as it offers no added-value to the diagnosis and management of MG.



Specimen Required


Only orderable as part of a profile. For more information see:

MGLE / Myasthenia Gravis/Lambert-Eaton Myasthenic Syndrome Evaluation, Serum

MGMR / Myasthenia Gravis Evaluation with Muscle-Specific Kinase (MuSK) Reflex, Serum

PAVAL / Paraneoplastic, Autoantibody Evaluation, Serum

 

Collection Container/Tube:

Preferred: Red top

Acceptable: Serum gel

Submission Container/Tube: Plastic vial

Specimen Volume: 1 mL

Collection Instructions: Centrifuge and aliquot serum into a plastic vial.


Specimen Minimum Volume

0.5 mL

Specimen Stability Information

Specimen Type Temperature Time
Serum Refrigerated (preferred) 28 days
  Frozen  28 days
  Ambient  72 hours
UPH Waterloo Region Lab Test Catalog Note:

Transport refrigerated.

Reject Due To

Gross hemolysis Reject
Gross lipemia Reject
Gross icterus Reject

Performing Laboratory

Mayo Clinic Laboratories in Rochester

Method Name

Only orderable as part of a profile. For more information see:

MGLE / Myasthenia Gravis/Lambert-Eaton Myasthenic Syndrome Evaluation, Serum

MGMR / Myasthenia Gravis Evaluation with Muscle-Specific Kinase (MuSK) Reflex, Serum

PAVAL / Paraneoplastic, Autoantibody Evaluation, Serum

 

Flow Cytometry

Useful For

Diagnosis for autoimmune myasthenia gravis (MG) in adults and children

 

Distinguishing autoimmune from congenital MG in adults and children or other acquired forms of neuromuscular junction transmission disorders.

 

This test is a qualitative assay and should not be used for monitoring purposes.

Day(s) Performed

Monday, Wednesday, Saturday

Report Available

5 to 8 days

Reference Values

Only orderable as part of a profile. For more information see:

MGLE / Myasthenia Gravis/Lambert-Eaton Myasthenic Syndrome Evaluation, Serum

MGMR / Myasthenia Gravis Evaluation with Muscle-Specific Kinase (MuSK) Reflex, Serum

PAVAL / Paraneoplastic, Autoantibody Evaluation, Serum

 

Negative

CPT Code Information

86043