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Myotomes

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Introduction

A myotome (Greek: myo = muscle; tome = a cut or slice) refers to the collection of muscle fibres innervated by motor axons within a single spinal nerve root.[1] Embryologically, myotomes originate from somites derived from the paraxial mesoderm and contribute to the development of skeletal muscle. This segmental organisation provides the developmental basis for the relationship between spinal nerve roots and the muscles they innervate.[1] Myotomes represent the motor component of the neurological examination and are commonly assessed through specific muscle actions and strength testing. In contrast, a dermatome represents an area of skin supplied predominantly by sensory fibres from a single spinal nerve root and is evaluated through sensory testing.[2] Together, assessment of myotomes, dermatomes, and reflexes can provide information about the neurological integrity of a spinal nerve root and assist with localisation of neurological dysfunction.

Figure 1: Differentiation of somites into dermatome, sclerotome and myotome showing embryological development of myotomes
Figure 1: Differentiation of somites into dermatome, sclerotome and myotome showing embryological development of myotomes

Anatomy

Figure 2: Spinal cord cross-section showing nerve root emergence and myotome innervation patterns

There are 31 pairs of spinal nerves: 8 cervical, 12 thoracic, 5 lumbar, 5 sacral, and 1 coccygeal. Although there are only seven cervical vertebrae, there are eight cervical spinal nerves; the C8 spinal nerve exits between the C7 and T1 vertebrae.[1]

Motor innervation of skeletal muscle originates from motor neurons within the spinal cord, whose axons exit through the ventral roots and join the dorsal roots to form mixed spinal nerves. These spinal nerves subsequently divide into rami, with the ventral rami contributing to nerve plexuses that ultimately give rise to the peripheral nerves supplying the muscles of the limbs.[1]

Within the nerve plexuses, fibres from adjacent spinal nerve roots intermingle and are redistributed into peripheral nerves. As a result, a peripheral nerve typically contains fibres originating from multiple spinal nerve roots, and an individual muscle may receive motor contributions from more than one spinal level. The relative contribution of each spinal nerve root to a muscle may differ, with one root often providing the predominant motor contribution.[1][3]

Myotome Distribution

Myotomal distributions describe the patterns of skeletal muscle innervation associated with individual spinal nerve roots. Although traditionally represented as specific roots corresponding to individual muscles or movements, human myotomes demonstrate considerable overlap, and the distribution of motor innervation may vary between individuals.[3][4]

Human myotomal distributions have been investigated using anatomical studies, clinical observations of nerve root lesions, electromyography, and direct electrical stimulation of spinal nerve roots.[3] Direct intraoperative nerve root stimulation has demonstrated that individual spinal nerve roots may activate a broader range of muscles than traditionally represented in standard myotome maps.[3][4] Similar findings have been demonstrated in the lumbosacral region, where broad motor distributions and individual and side-to-side variation in root contributions have been identified.[5]

It is important to distinguish a myotomal pattern from a peripheral nerve distribution.[1] A spinal nerve root contributes motor fibres to multiple peripheral nerves; therefore, muscles sharing the same predominant root innervation may be supplied by different peripheral nerves. Conversely, an individual peripheral nerve typically contains fibres originating from multiple spinal nerve roots. Assessment of weakness across muscles supplied by different peripheral nerves but sharing a common spinal nerve root can therefore assist in localising neurological dysfunction to the nerve root rather than to an individual peripheral nerve.[3][6]

For example, the C5 spinal nerve root contributes to both the axillary nerve, which supplies the deltoid, and the musculocutaneous nerve, which supplies the biceps brachii. Consequently, C5 nerve root dysfunction may produce weakness in both shoulder abduction and elbow flexion despite these muscles being supplied by different peripheral nerves. This pattern can assist in distinguishing C5 nerve root involvement from an isolated axillary or musculocutaneous neuropathy.[3][6]

Consequently, due to overlapping innervation and anatomical variation, clinical myotome maps should be interpreted as representations of predominant patterns of motor innervation rather than fixed anatomical territories.[3][4][5]

ISNCSCI Standardized Key Muscle Functions

The International Standards for Neurological Classification of Spinal Cord Injury (ISNCSCI) identifies 10 bilateral key muscle functions for standardised motor examination. Each key muscle function is associated with a spinal cord segment and is tested using a defined movement and muscle group. These key muscle functions are used for neurological classification of spinal cord injury and should not be interpreted as exclusive anatomical myotomal distributions.[7]

Table 1: Key Muscle Functions - ISNCSCI Standard[7]
Spinal Nerve Root Key Muscle Function Representative Muscle(s)
C5 Elbow flexion Biceps brachii

Brachialis

C6 Wrist extension Extensor carpi radialis longus/brevis
C7 Elbow extension Triceps
C8 Finger flexion Flexor digitorum profundus
T1 Small finger abductors Abductor digiti minimi
L2 Hip flexion Iliopsoas
L3 Knee extension Quadriceps
L4 Ankle dorsiflexion Tibialis anterior
L5 Long toe extension Extensor hallucis longus
S1 Ankle plantarflexion Gastrocnemius

Soleus

S2-S4 Anal sphincter contraction

Clinical note: ISNCSCI key muscle functions provide a standardised method for assessing motor function following spinal cord injury. Because most muscles receive innervation from more than one spinal nerve root, these key muscle functions should not be considered exclusive root-to-muscle relationships.[3][7]

Clinical Myotomal Distribution

The ISNCSCI key muscle functions provide a standardised approach to motor examination; however, they do not represent the full distribution of motor innervation associated with each spinal nerve root. Studies using clinical observations, electromyography, and direct intraoperative nerve root stimulation demonstrate considerable overlap between adjacent myotomes, with individual spinal nerve roots contributing to multiple muscles and movements.[3][4]

The following tables summarise commonly recognised and predominant myotomal relationships for the upper and lower limbs. These distributions should be used as a clinical guide rather than interpreted as fixed anatomical boundaries.[3][4][5]

Table 2: Cervical and Upper Limb Myotomal Distribution
Spinal Nerve Root Commonly Associated Movement(s) Representative Muscle(s) Peripheral Nerve(s)
C5 Shoulder abduction

Elbow flexion

Deltoid

Biceps brachii

Axillary

Musculocutaneous

C6 Elbow flexion

Wrist extension Forearm pronation

Biceps brachii

Brachioradialis

Exensor carpi radialis longus/brevis

Pronator teres

Musculocutaneous

Radial

Median

C7 Elbow extension

wrist flexion Finger extension

Triceps

Flexor carpi radialis

Finger extensors

Radial

Median

C8 Finger flexion

Thumb/finger extension

Flexor digitorum profundus

Extensor pollicis longus

Finger extensors

Median

Ulnar

Radial

T1 Finger abduction/adduction Interossei

Abductor digiti minimi

Ulnar
Table 3: Lumbosacral and Lower Limb Myotomal Distribution
Spinal Nerve Root Commonly Associated Movement(s) Representative Muscle(s) Peripheral Nerve(s)
L2 Hip flexion Iliopsoas Femoral/direct lumbar plexus branches
L3 Knee extension

Hip adduction

Quadriceps

Adductors

Femoral

Obturator

L4 Knee extension

Ankle dorsiflexion

Quadriceps

Tibialis anterior

Femoral

Deep fibular

L5 Great toe extension

Ankle dorsiflexion Hip abduction

Extensor hallucis longus

Tibialis anterior

Gluteus medius

Deep fibular

Deep fibular

Superior gluteal

S1 Ankle plantarflexion

Ankle eversion

Gastrocnemius

Soleus

Fibularis longus/brevis

Tibial

Superficial fibular

S2 Knee flexion Hamstrings Sciatic

Clinical interpretation: Weakness involving several muscles supplied by different peripheral nerves but sharing a common spinal nerve root may be more suggestive of a radicular pattern than weakness confined to the distribution of a single peripheral nerve.[6] Significant overlap and individual variation exist; therefore, findings should be interpreted alongside sensory examination, reflexes, and other clinical findings rather than used in isolation.[3][4][5]

Assessment

Purpose

Myotomal strength is typically assessed through isometric resisted muscle testing with findings used to assist in identifying the presence and potential level of nerve root involvement.[8][9] Assessment of multiple muscles can also assist with neurological localisation. Weakness affecting muscles supplied by different peripheral nerves but sharing a common spinal nerve root may support a radicular pattern, whereas weakness limited to muscles supplied by a single peripheral nerve may suggest a more distal peripheral nerve lesion.[6]

Myotomal testing should not be interpreted in isolation. Motor testing has demonstrated variable diagnostic accuracy and generally limited sensitivity for detecting radiculopathy; therefore, normal muscle strength does not necessarily exclude nerve root involvement. Findings should be interpreted alongside the patient's history and other components of the neurological examination, including sensory testing and reflexes.[8][9][10] Muscle strength may be documented using a standardised muscle strength grading scale.

Medical Research Council (MRC) Muscle Strength Grading Scale

Table 4: MRC Muscle Strength Scale[11]
Grade Description
0 No contraction
1 Flicker or trace of contraction
2 Active movement with gravity eliminated
3 Active movement against gravity
4 Active movement against gravity and resistance
5 Normal power

Technique

Myotomal testing is commonly performed using resisted isometric muscle testing. The patient is positioned to isolate the movement being assessed and instructed to hold the position while the examiner applies resistance. One commonly described clinical approach uses resisted isometric contraction maintained for approximately 5 seconds, while assessing for weakness and comparing the response with the contralateral side.[12]

Testing should be performed bilaterally, simultaneously using consistent positioning, stabilisation, and resistance.[7] The examiner should assess for differences in strength between sides and consider whether weakness follows a pattern consistent with involvement of a spinal nerve root. Muscle strength may be documented using the Medical Research Council (MRC) muscle strength scale as listed above in Table 4.[11]

Table 5 includes common Myotomal Testing Techniques used in current literature:

Table 5: Myotomal Testing Techniques (Adapted from [7][12])
Root Test Movement Patient Testing Position

Anti-Gravity

Patient Testing Position

Gravity Eliminated

Resistance/Examiner Action (Anti-Gravity)
C5 Shoulder abduction Sitting Sidelying Examiner applies downward force proximal to elbow into adduction
C6 Elbow flexion & wrist extension Sitting (both) Elbow flexion: Sidelying

Wrist extension: Sitting

Elbow flexion: Examiner applies resistance at wrist to extend the elbow

Wrist extension: Examiner applies resistance on dorsum of hand into wrist flexion.

C7 Elbow extension & wrist flexion Sitting (both) Elbow extension: Sidelying

Wrist flexion: Sitting

Elbow extension: Examiner applies resistance at wrist to flex the elbow.

Wrist flexion: Examiner applies resistance on palm of hand into wrist extension.

C8 Finger flexion Sitting Sitting Examiner applies resistance to distal phalanx into extension
T1 Finger abduction Sitting Sitting Examiner applies resistance into finger adduction
L2 Hip flexion Sitting Sidelying Patient flexes hip in sitting while examiner applies resistance into hip extension
L3 Knee extension Sitting Sidelying Patient extends their knee 20 degrees from full extension and examiner applies resistance into flexion
L4 Ankle dorsiflexion Sitting Sidelying Patient dorsiflexes their ankle while examiner applies resistance into plantar flexion
L5 Great toe extension Sitting or Supine Examiner applies resistance at distal phalanx into great toe flexion
S1 Ankle plantarflexion and eversion Ankle plantarflexion: Prone or standing Sidelying (both) Ankle plantarflexion: Examiner applies resistance into ankle dorsiflexion
S2 Knee flexion Prone Sidelying Patient flexes the knee to 90 degrees and examiner applies resistance into knee extension
S2-4 Anal sphincter contraction Prone Prone The examiner inserts a gloved finger into the patient's rectum and graded as being present or absent.

The instruction to the patient should be “squeeze my finger as if to hold back a bowel movement"

Repeated Testing

A single strength assessment may not identify all motor deficits associated with nerve root dysfunction. Emerging evidence suggests that repeated muscle contractions may reveal fatigable weakness that is not apparent during initial strength testing, potentially providing additional information when nerve root involvement is suspected despite normal or near-normal strength. However, evidence supporting repeated or endurance-based myotomal testing remains limited, and this approach has not been established as a standardised component of the neurological examination.[13]

Diagnostic Accuracy

The diagnostic performance of myotomal testing varies depending on the spinal level assessed, testing procedure, and reference standard. Overall, motor testing appears to demonstrate limited sensitivity, indicating that normal muscle strength does not reliably exclude nerve root involvement.[8][9]

In patients with surgically verified single-level cervical radiculopathy, objective motor weakness was identified in 48.5% of patients. Among patients demonstrating motor weakness, approximately two-thirds followed the expected standard myotomal pattern, with variation observed between cervical nerve root levels. Notably, greater variability was observed with C5/6 level (C6 root) radiculopathy.[14] These findings demonstrate that motor weakness may assist with localisation but does not always correspond to traditional myotomal distributions.

The diagnostic accuracy of the neurological examination may improve when motor findings are considered alongside other neurological findings. In cervical radiculopathy, combinations of muscle weakness, sensory loss, and tendon reflex abnormalities have demonstrated higher specificity than some individual examination components, although sensitivity remains variable.[8] For lumbosacral radiculopathy, motor testing has demonstrated poor-to-moderate sensitivity, ranging from 0.13 to 0.61 across included studies.[9] Therefore, myotomal findings are best interpreted as one component of the broader neurological examination rather than as an independent diagnostic test.

Clinical relevance

Myotomal assessment contributes to the evaluation of patients with possible neurological involvement and can help clinicians recognise patterns of motor weakness and localise potential dysfunction within the nervous system.[3] When a weakness occurs across muscles innervated by different peripheral nerves but shares a common spinal root, the pattern can help assist clinicians in determining and distinguishing a radiculopathy from a peripheral mononeuropathy.[6]

Myotomal findings may also contribute in identifying the potential level of nerve root involvement and determining the need for further investigation or referral. However, patterns of weakness do not always correspond precisely with traditional myotome maps because of overlapping innervation and individual anatomical variation.[3][14] As a result, myotomal findings should be interpreted in conjunction with a battery of tests including patient's history, sensory examination, reflexes, and other relevant clinical findings rather than used independently to establish a diagnosis.[8][9]

References

  1. ↑ 1.0 1.1 1.2 1.3 1.4 1.5 Standring S. Gray's Anatomy: The Anatomical Basis of Clinical Practice. 42nd ed. London: Elsevier; 2020.
  2. ↑ Lee MWL, McPhee RW, Stringer MD. An evidence-based approach to human dermatomes. Clin Anat. 2008;21(5):363-73.
  3. ↑ 3.00 3.01 3.02 3.03 3.04 3.05 3.06 3.07 3.08 3.09 3.10 3.11 3.12 Sonoo M. Recent advances in neuroanatomy: the myotome update. J Neurol Neurosurg Psychiatry. 2023;94(8):643-8.
  4. ↑ 4.0 4.1 4.2 4.3 4.4 4.5 Schirmer CM, Shils JL, Arle JE, Cosgrove GR, Dempsey PK, Tarlov E, et al. Heuristic map of myotomal innervation in humans using direct intraoperative nerve root stimulation. J Neurosurg Spine. 2011;15(1):64-70. doi:10.3171/2011.2.SPINE1068
  5. ↑ 5.0 5.1 5.2 5.3 Hashimoto S, Murohashi T, Yamada S, Iesato N, Ogon I, Chiba M, et al. Broad and asymmetric lower extremity myotomes: results from intraoperative direct electrical stimulation of the lumbosacral spinal roots. Spine (Phila Pa 1976). 2024;49(11):805-10.
  6. ↑ 6.0 6.1 6.2 6.3 6.4 Robblee J, Katzberg H. Distinguishing radiculopathies from mononeuropathies. Front Neurol. 2016;7:111.
  7. ↑ 7.0 7.1 7.2 7.3 7.4 Rupp R, Biering-Sørensen F, Burns SP, Graves DE, Guest J, Jones L, et al. International Standards for Neurological Classification of Spinal Cord Injury: Revised 2019. Top Spinal Cord Inj Rehabil. 2021;27(2):1-22.
  8. ↑ 8.0 8.1 8.2 8.3 8.4 Yousif MS, Occhipinti G, Bianchini F, Feller D, Schmid AB, Mourad F. Neurological examination for cervical radiculopathy: a scoping review. BMC Musculoskelet Disord. 2025;26:334.
  9. ↑ 9.0 9.1 9.2 9.3 9.4 Tawa N, Rhoda A, Diener I. Accuracy of clinical neurological examination in diagnosing lumbo-sacral radiculopathy: a systematic literature review. BMC Musculoskelet Disord. 2017;18:93.
  10. ↑ Wainner RS, Fritz JM, Irrgang JJ, et al. Reliability and diagnostic accuracy of the clinical examination and patient self-report measures for cervical radiculopathy. Spine. 2003;28(1):52-62. Available from: https://journals.lww.com/spinejournal/abstract/2003/01010/reliability_and_diagnostic_accuracy_of_the.10.aspx
  11. ↑ 11.0 11.1 Compston A. Aids to the investigation of peripheral nerve injuries. Medical Research Council: Nerve Injuries Research Committee. His Majesty's Stationery Office: 1942; pp. 48 (iii) and 74 figures and 7 diagrams; with Aids to the Examination of the Peripheral Nervous System. By Michael O'Brien for the Guarantors of Brain. Saunders Elsevier: 2010; pp. [8] 64 and 94 figures. Brain. 2010;133(10):2838-44.
  12. ↑ 12.0 12.1 Magee DJ. Orthopedic physical assessment. 7th ed. St. Louis (MO): Elsevier; 2021.
  13. ↑ Coulombe-Lévêque A, Dehors N, Pelletier R, Cabana F, Dumas JP, Léonard G. Strength vs. endurance in myotome assessment—a case for (further studies on) repeated measurements. Front Rehabil Sci. 2026;7:1670617.
  14. ↑ 14.0 14.1 Hong CG, Nam WD. Reliability and diagnostic accuracy of standard dermatomes and myotomes for determining the pathologic level in surgically verified patients with cervical radiculopathy. Neurospine. 2022;19(4):1006-12.