Differentials

Tetany

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Produces a characteristic motor posture known as carpopedal spasm.

Hypocalcemic tetany: tingling begins around the mouth and in the peripheral extremities, then increases in intensity and spreads proximally. A sensation of spasm or tension follows the same pattern as the tingling, eventually producing a tonic spasm. If severe, proximal and paraspinal muscles may be involved. Laryngeal muscles are commonly involved early. On exam, positive Trousseau sign and Chvostek sign are suggestive of neural hyperexcitability.

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Typical clinical findings with an associated electrolyte abnormality (either hypocalcemia, hypomagnesemia, or alkalosis).

There may also be hypokalemia or hyperkalemia.

Electromyogram findings: individual motor units discharge independently at a rate of 5 to 25 Hz (each discharge is a group of ≥2 identical potentials).

Tetanus

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Primary symptoms are muscular rigidity and spasms. Trismus and dysphagia are typical.

The spasms, which are extremely painful, are caused by sudden, involuntary contractions of opposing muscles that last for only a few seconds, but occur repeatedly for minutes.

Spasms are localized or generalized and can be triggered by sensory stimuli, movement, or emotion.

In some cases, spasms are severe enough to cause muscle injury or to fracture bones.

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Diagnosed clinically.

No specific change found in blood, urine, or cerebrospinal fluid.

No specific confirmatory laboratory test (absence of serum tetanus toxin or a negative result from clostridial culture testing does not rule out infection).

Occupational cramps

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Muscular contractions without pain.

A type of dystonia and not cramp.

Task-specific, arising due to repetitive or skilled use of a body part (e.g., hands [hairstylists, musicians, court reporters], mouth [musicians playing wind instruments]).

Begin in adulthood.[89]

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No distinguishing tests.

Restless legs syndrome

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Urge to move legs with or without paresthesias when relaxing or attempting to sleep. Resolves when patient begins activity.[90] Muscle hardening is not usually present.

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No differentiating tests.

Growing pains

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Not associated with palpable/visible hardening of muscle usually seen with cramps.

Most common sites of pain are shins and calves.

Pain lasts between a few minutes and a few hours.

Occurs at night and usually disappears by the morning.[91]

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No differentiating tests.

Neuromyotonia (e.g., Isaac syndrome)

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Predisposes to true muscle cramps.

However, other clinical manifestations of this disorder of continuous muscle fiber activity are usually even more prominent.

All cases of neuromyotonia have visible continuous muscle "worm-like movements" (myokymia).

Abnormal limb posturing, identical to carpal or pedal spasm, are characteristic and may be persistent or intermittent.

There is difficulty in relaxing the muscle (which differs from true myotonia), a lack of percussion myotonia, and increased rather than decreased stiffness with continued activity.

In children and young adults, it progresses insidiously.

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Associated with the presence of serum antibodies to voltage-gated potassium channels.

Continuous muscle fiber activity syndromes (not neuromyotonia)

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Slow muscle relaxation after contraction as well as nonmuscular findings (autonomic findings [e.g., hyperhidrosis, hypersalivation, and hyperlacrimation]).

May be associated with autoimmune phenomena, such as myasthenia gravis and thymoma.[92]

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EMG demonstrates myokymic and neuromyotonic discharges.

Autoantibodies to antigens on peripheral motor neurons and autonomic fibers.

Multiple sclerosis

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Common symptoms include visual disturbance, sensory phenomena (e.g., sensations of wetness or burning, hemibody sensory loss or tingling, Lhermitte sign [electric shock-like sensations extending down the cervical spine radiating to the limbs]), progressive limb weakness, gait difficulty, ataxia, sphincter and sexual dysfunction, fatigue.

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Brain MRI with gadolinium enhancement typically shows areas of demyelination; sagittal fluid-attenuated inversion recovery images are the most sensitive.

Cerebrospinal fluid (CSF) analysis: oligoclonal bands and elevated CSF IgG and IgG synthesis rate may be present.

Somatosensory, visual evoked, and brainstem auditory evoked potentials are prolonged.

Dystrophinopathies (e.g., Duchenne or Becker muscular dystrophy)

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May be a family history of the condition.

Loss of ability to walk by about 12 years old (Duchenne).

Contractures of hips, knees, ankles. Severe scoliosis.[88]

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DNA studies may detect deletion of dystrophin gene.

Abnormal ECG due to degeneration and fibrosis of posterolateral aspect of left ventricular wall.

Echocardiogram may show abnormal valve and wall motion, cardiomyopathy.

Serum CK levels are markedly increased.

EMG may reveal myopathic changes.

Muscle biopsy may show variation in fiber sizes, fibrosis, basophilic and hyaline fibers in groups.

Myotonic dystrophies

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Myotonia is characterized by slowing in the relaxation of muscles after voluntary contraction or electrical stimulation.

Dystrophies characterized by weakness of hand, feet, neck muscles; hollowing of temples due to masseter and temporalis atrophy.

Shoulder, hip, leg weakness can lead to repeated falls.

Demonstration of myotonia by sharp percussion of muscle with reflex hammer or after firm voluntary contraction.

Cardiomyopathy; excessive daytime somnolence and cataracts.[88]

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DNA studies may detect mutations of myotonic muscular dystrophy protein kinase (DMPK) gene.

Muscle biopsy may show variability in fiber size, fibrosis, and ring fibers.

EMG may show myotonic discharges (repetitive firing of muscle fibers at 20 to 80 Hz with waxing/waning of the amplitude/frequency).

Satoyoshi syndrome

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Alopecia, diarrhea, endocrinopathy with amenorrhea, and secondary skeletal abnormalities, in addition to painful muscle spasms.[93]

Syndrome usually develops between 6 and 15 years of age, with alopecia and leg spasms initially.

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Clinical diagnosis.

Brody disease

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Difficulty with walking and climbing stairs.

Enhanced fatigability during exercise.

Painless contractures (stiffness) during exercise.

Increased exercise intolerance in cold environment.[94][95][96]

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Muscle biopsy may be sent for analysis of microsomal calcium uptake, which shows a significant decrease compared with controls.

EMG shows impaired relaxation of agonist muscles, with substantial electrical activity of antagonist muscles at the same time.

DNA analysis detects deficiency of gene for sarcoplasmic reticulum ATP-dependent calcium pump.

Swartz-Jampel syndrome

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Facial malformations (microstomia, micrognathia, retrognathia, short palpebral fissures, low-set ears, short neck).

Musculoskeletal signs, including myopathy, myotonia, muscle hypertrophy, restricted joint mobility, kyphosis, scoliosis, pectus carinatum, anterior bowing of long bones.

Areflexia or hyporeflexia, cognitive dysfunction.[97]

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DNA analysis for gene causing abnormal proteoglycan of basement membranes.

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