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Limb weakness

Epidemiology

Epidemiology

  • Limb weakness is a common presenting symptom in neurology and general practice, affecting individuals of all ages.
  • The prevalence increases with age, with a higher incidence in patients with comorbid conditions such as diabetes, stroke, and multiple sclerosis.
  • It can result from a wide range of conditions, from benign to life-threatening, necessitating careful evaluation.
  • Limb weakness can be due to central nervous system disorders, peripheral nervous system disorders, muscle diseases, or systemic conditions.
  • The burden of disease varies globally, with higher rates in populations with limited access to healthcare and higher rates of vascular risk factors.

Differential Diagnosis Schema 🧠

Central Nervous System Causes

  • Stroke: Sudden onset of limb weakness, typically unilateral, with or without other neurological deficits.
  • Multiple Sclerosis: Relapsing-remitting weakness, often associated with other symptoms like optic neuritis and sensory changes.
  • Spinal Cord Compression: Can cause bilateral limb weakness, often with sensory changes below the level of the lesion.
  • Brain Tumor: Gradual onset of limb weakness, often with other signs of raised intracranial pressure.
  • Cerebral Palsy: Non-progressive motor disorder beginning in early childhood, characterized by spasticity and limb weakness.
  • Motor Neuron Disease (ALS): Progressive weakness with muscle atrophy and fasciculations, usually starting distally.
  • Transverse Myelitis: Acute or subacute spinal cord inflammation causing bilateral limb weakness, often with bowel/bladder dysfunction.
  • Cerebral Palsy: Non-progressive motor disorder from early childhood, characterized by spasticity and limb weakness.
  • Guillain-BarrΓ© Syndrome: Ascending, symmetrical weakness, often following an infection, with absent reflexes.
  • Parkinson’s Disease: Limb weakness as part of generalized bradykinesia, rigidity, and tremor.

Peripheral Nervous System Causes

  • Peripheral Neuropathy: Commonly caused by diabetes, presenting with distal limb weakness and sensory loss.
  • Radiculopathy: Compression of nerve roots, often causing unilateral limb weakness with radicular pain.
  • Carpal Tunnel Syndrome: Median nerve compression leading to weakness and atrophy of the thenar muscles.
  • Bell’s Palsy: Facial nerve paralysis causing weakness of the muscles on one side of the face.
  • Myasthenia Gravis: Autoimmune disorder causing fluctuating muscle weakness, often worsened by activity and improved by rest.
  • Polyneuropathy: Often seen in conditions like chronic alcoholism, leading to symmetric distal limb weakness.
  • Diabetic Amyotrophy: A painful, asymmetrical motor neuropathy affecting the thighs and hips, seen in diabetics.
  • Entrapment Neuropathy: Compression of peripheral nerves (e.g., ulnar or radial nerves) leading to localized limb weakness.

Muscular Causes

  • Muscular Dystrophy: Genetic disorders causing progressive muscle weakness and wasting, often starting in childhood.
  • Polymyositis: Inflammatory myopathy causing proximal muscle weakness and raised muscle enzymes.
  • Dermatomyositis: Similar to polymyositis, but with characteristic skin rashes.
  • Rhabdomyolysis: Muscle breakdown leading to weakness, myoglobinuria, and raised creatine kinase.
  • Inclusion Body Myositis: A slowly progressive inflammatory myopathy affecting the elderly, with both proximal and distal muscle weakness.
  • Statin-induced Myopathy: Muscle weakness and pain caused by statin use, usually reversible upon cessation.
  • Hypokalemic Periodic Paralysis: A rare condition causing episodic muscle weakness due to low potassium levels.
  • Thyrotoxic Myopathy: Muscle weakness due to hyperthyroidism, often improving with treatment of the underlying condition.
  • Fibromyalgia: Chronic condition characterized by widespread pain, fatigue, and muscle tenderness, sometimes perceived as weakness.
  • Myotonic Dystrophy: Genetic disorder causing muscle stiffness (myotonia) and weakness, along with systemic features.

Key Points in History πŸ₯Ό

Background

  • Onset and Duration: Determine whether the weakness is acute, subacute, or chronic.
  • Progression: Ask about how the weakness has progressed and whether it is fluctuating or steadily worsening.
  • Symmetry: Ascertain whether the weakness is unilateral, bilateral, or asymmetric.
  • Associated Symptoms: Inquire about pain, sensory changes, sphincter disturbances, or systemic symptoms like fever or weight loss.
  • Risk Factors: Identify risk factors such as recent infections, vaccination, trauma, or exposure to toxins.
  • Family History: Ask about any family history of neurological or muscular diseases.
  • Medication History: Note any medications that could contribute to weakness, such as statins or steroids.
  • Past Medical History: Include relevant conditions such as diabetes, vascular disease, or previous strokes.
  • Social History: Consider occupational exposure, physical activity levels, and substance use.
  • Functional Impact: Assess how the weakness affects daily activities, mobility, and independence.
  • Psychiatric History: Explore any history of mental health issues, as depression and anxiety can present with perceived weakness.

Possible Investigations 🌑️

Clinical Examination

  • Neurological Examination: Assess muscle strength, tone, reflexes, and coordination to localize the lesion.
  • Sensory Examination: Check for sensory deficits, which can help differentiate between central and peripheral causes.
  • Gait Assessment: Observe the patient’s gait for any abnormalities that could suggest a specific diagnosis.
  • Cranial Nerve Examination: Particularly important in cases where the weakness is associated with facial or bulbar symptoms.
  • Cardiovascular Examination: To rule out vascular causes such as stroke or peripheral arterial disease.
  • Musculoskeletal Examination: Check for signs of joint inflammation, muscle atrophy, or tenderness.
  • Skin Examination: Look for rashes, ulcers, or other dermatological signs that could suggest systemic disease.
  • Respiratory Examination: Consider in cases where weakness is associated with conditions like Guillain-BarrΓ© Syndrome.

Laboratory Tests

  • Full Blood Count (FBC): To identify any underlying infection, anemia, or hematological cause.
  • Electrolytes: Particularly potassium, calcium, and magnesium, which can affect muscle function.
  • Thyroid Function Tests: To rule out hypothyroidism or hyperthyroidism as causes of muscle weakness.
  • Creatine Kinase (CK): Elevated in muscle diseases such as polymyositis or rhabdomyolysis.
  • Autoantibodies: For suspected autoimmune conditions like myasthenia gravis or lupus.
  • ESR/CRP: Elevated in inflammatory or infectious conditions causing limb weakness.
  • Vitamin B12 and Folate: Deficiencies can lead to peripheral neuropathy and weakness.
  • Toxicology Screen: Consider in cases of suspected drug or toxin-induced weakness.
  • Lactate and Pyruvate: To evaluate for mitochondrial disorders if suspected.
  • Lumbar Puncture: Consider in cases of suspected Guillain-BarrΓ© Syndrome or CNS infection.
  • Electromyography (EMG) and Nerve Conduction Studies: Useful in diagnosing neuromuscular disorders.
  • Genetic Testing: For conditions such as muscular dystrophy or myotonic disorders.

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