Skip to content
PubMed This is a summary of 10 peer-reviewed journal articles Updated
Neurology · Myotonia

What Do Myotonic Discharges on an EMG Sound Like?

At a Glance

On an EMG, myotonic discharges sound like a "dive bomber" airplane or a revving motorcycle engine. This distinct waxing and waning noise happens because hyperexcitable muscles fail to relax normally, continuing to fire electrical signals that rapidly change in pitch and volume.

During an electromyography (EMG) test, myotonic discharges create a very distinct sound that neurologists often compare to a “dive bomber” airplane or a revving motorcycle engine [1][2]. This occurs because the EMG machine translates the electrical activity of your muscles into an audio signal you can hear in the exam room. When a muscle with myotonia tries to relax, it continues to fire off electrical signals that rise and fall in speed and volume, creating that characteristic revving or dropping pitch [1][2]. While hearing loud, erratic noises coming from your own body during a medical test can be startling, the sound itself is completely harmless.

How the EMG “Hears” Your Muscles

An electromyogram (EMG) is a diagnostic test that measures the electrical health of your muscles and the nerves that control them. During the needle portion of the exam, the doctor inserts a tiny, thin pin into a specific muscle. This needle acts like an electrical antenna.

Muscle cells communicate and move using electricity. The EMG machine captures these tiny electrical impulses and converts them into visual waves on a screen, as well as audible sounds through a speaker. This allows the neurologist to literally “listen” to how your muscles behave when they are resting and when they contract. While you might feel a pinch or mild cramping from the needle itself, the sound you hear is simply the machine translating these electrical signals.

The Anatomy of the “Dive Bomber” Sound

In a healthy muscle, the electrical signals fall completely silent as soon as you relax the muscle. However, in conditions like myotonic dystrophy, the muscle cells are hyperexcitable—meaning their outer membranes are unstable and prone to firing off signals even when they shouldn’t [3].

If you have myotonia, the muscle cells have a hard time stopping their electrical activity after a contraction, or sometimes even just from the minor irritation of the needle entering the muscle. Instead of going quiet, the muscle continues to fire repetitive electrical signals [1]. It is important to know that the needle temporarily irritating the muscle to cause this response is a normal part of the test and does not cause permanent muscle damage.

The “dive bomber” sound happens because of two simultaneous changes in these extra signals:

  • Frequency (Pitch): The speed of the electrical firing speeds up and then slows down.
  • Amplitude (Volume): The size of the electrical signals gets larger, then smaller.

Doctors call this rising and falling pattern “waxing and waning” [1][2]. Just like a motorcycle engine revving up and then winding down, or an airplane diving out of the sky, the pitch and volume of your muscle’s electrical activity peaks and fades out over a few seconds [2].

What This Sound Means for Your Diagnosis

Hearing this “dive bomber” sound is a key diagnostic clue for your neurologist. It is the hallmark electrodiagnostic sign of myotonia—the delayed relaxation of a muscle after you use it [2][4].

  • Confirming the condition: While you might feel stiffness or notice that it’s hard to let go of a doorknob, the EMG sound provides objective, medical proof that the stiffness is caused by electrical myotonia rather than joint pain or a different muscle issue [4].
  • Guiding the diagnosis: Myotonic discharges are most commonly associated with genetic conditions like myotonic dystrophy (both Type 1 and Type 2) and non-dystrophic myotonias [5][6]. However, they can occasionally be seen in other muscle conditions, such as toxic myopathies from certain medications or inflammatory disorders [7][4]. This is why hearing this sound likely led your care team to recommend genetic testing to confirm your specific diagnosis [8].

It is important to know that the volume or length of the “dive bomber” sounds on your EMG does not perfectly match how stiff your muscles feel in your daily life [2][9]. You can have significant myotonic sounds on an EMG but only experience mild stiffness, or vice versa [10].

Common questions in this guide

Why does an EMG machine make noise?
An EMG machine acts like an electrical antenna that captures the tiny electrical impulses from your muscles. It then translates these signals into visual waves on a screen and audible sounds through a speaker, allowing the neurologist to listen to how your muscles behave.
What does the "dive bomber" sound mean on my EMG?
The dive bomber sound is a classic sign of myotonia, which means delayed muscle relaxation. It occurs when a muscle's electrical signals speed up and slow down, causing the pitch and volume of the sound to rise and fall.
Does the volume of the EMG sound relate to how stiff my muscles feel?
No, the volume or length of the myotonic sounds on an EMG does not perfectly match your daily symptoms. You might have significant EMG sounds but only experience mild stiffness, or vice versa.
Can the needle used in an EMG cause permanent muscle damage?
While the needle used during an EMG exam temporarily irritates the muscle to capture electrical signals, it is a normal part of the test. It is safe and does not cause any permanent damage to your muscle.

Questions to Ask Your Doctor

Curated prompts to bring to your next appointment.

  1. 1.Did you hear the myotonic discharges in all the muscles you tested, or just specific ones?
  2. 2.Based on the EMG results, are there signs of both myotonia and muscle weakness (myopathy)?
  3. 3.Does the specific pattern of my dive bomber sounds change my treatment options?
  4. 4.Now that we have these results, do I ever need to undergo another EMG to track my disease?

Questions For You

Tap a prompt to share your answer — we'll use it plus this page's context to start a tailored conversation.

References

References (10)
  1. 1

    Myotonic Dystrophy.

    Perez PG

    Continuum (Minneapolis, Minn.) 2025; (31(5)):1437-1461 doi:10.1212/cont.0000000000001621.

    PMID: 41037177
  2. 2

    Myotonic disorders: A review article.

    Hahn C, Salajegheh MK

    Iranian journal of neurology 2016; (15(1)):46-53.

    PMID: 27141276
  3. 3

    Functional analysis of the F337C mutation in the CLCN1 gene associated with dominant myotonia congenita reveals an alteration of the macroscopic conductance and voltage dependence.

    Jehasse K, Jacquerie K, de Froidmont A, et al.

    Molecular genetics & genomic medicine 2021; (9(2)):e1588 doi:10.1002/mgg3.1588.

    PMID: 33507632
  4. 4

    Normal and abnormal spontaneous activity.

    Rubin DI

    Handbook of clinical neurology 2019; (160()):257-279 doi:10.1016/B978-0-444-64032-1.00017-5.

    PMID: 31277853
  5. 5

    Male infertility with muscle weakness: a point of view.

    Khalayli N, Achmeh B, Ali K, et al.

    Annals of medicine and surgery (2012) 2023; (85(10)):5120-5122 doi:10.1097/MS9.0000000000001147.

    PMID: 37811075
  6. 6

    Guidelines on clinical presentation and management of nondystrophic myotonias.

    Stunnenberg BC, LoRusso S, Arnold WD, et al.

    Muscle & nerve 2020; (62(4)):430-444 doi:10.1002/mus.26887.

    PMID: 32270509
  7. 7

    Colchicine-Induced Acute Myopathy: Case Study From Saudi Arabia.

    Al Megalli M, Bashir S, Qadah H, et al.

    Cureus 2021; (13(12)):e20290 doi:10.7759/cureus.20290.

    PMID: 35028201
  8. 8

    Special electromyographic features in a child with paramyotonia congenita: A case report and review of literature.

    Yi H, Liu CX, Ye SX, Liu YL

    World journal of clinical cases 2024; (12(3)):587-595 doi:10.12998/wjcc.v12.i3.587.

    PMID: 38322461
  9. 9

    Predominantly myalgic phenotype caused by the c.3466G>A p.A1156T mutation in SCN4A gene.

    Palmio J, Sandell S, Hanna MG, et al.

    Neurology 2017; (88(16)):1520-1527 doi:10.1212/WNL.0000000000003846.

    PMID: 28330959
  10. 10

    [A pedigree of myotonia congenita with a novel mutation p.F343C of the CLCN1 gene].

    Nakamura Y, Sato H, Kakiuchi K, et al.

    Rinsho shinkeigaku = Clinical neurology 2024; (64(5)):344-348 doi:10.5692/clinicalneurol.cn-001929.

    PMID: 38644209

This page explains EMG electrodiagnostic findings for educational purposes only. Always consult your neurologist to fully interpret your specific diagnostic test results and diagnosis.

Get notified when new evidence is published on Myotonic dystrophy.

We monitor PubMed for new peer-reviewed studies on this topic and email a short summary when something meaningful changes.