Symptom

Muscle weakness

Subjective or measurable loss of muscle strength — distinct from generalised fatigue. Causes range from electrolyte imbalance to myopathy to neurological disease; lab work clusters around electrolytes, thyroid, kidney, vitamin D and CK.

What it means

True muscle weakness — reduced ability to generate force when you try — must be separated from fatigue (decreased endurance with preserved peak strength) and from feeling weak as a synonym for tired. The pattern matters: proximal weakness (difficulty rising from a chair, climbing stairs, raising arms above the head) suggests myopathy or endocrine cause; distal weakness (gripping, foot drop) suggests neuropathy; fluctuating weakness that worsens with use is myasthenia gravis. Important treatable causes: electrolyte disturbance (low potassium, low calcium, low magnesium, low sodium, low phosphate), hypothyroidism (proximal), hyperparathyroidism, hypercortisolism, vitamin D deficiency (proximal), statins and other myotoxic drugs, chronic kidney disease (uraemic myopathy), inflammatory myopathies (dermatomyositis, polymyositis), and motor neurone disease.

Common causes

  • Hypokalaemia, hypocalcaemia, hypomagnesaemia, hyponatraemia — sudden onset; check on first presentation.
  • Hypothyroidism — proximal weakness + slow reflexes + fatigue.
  • Vitamin D deficiency — proximal weakness, especially elderly and dark-skinned.
  • Statin myopathy — calf aches + weakness; check CK.
  • Chronic kidney disease (uraemic myopathy) — proximal weakness + raised creatinine.
  • Cushing's, steroid use — proximal weakness + central obesity + skin changes.
  • Polymyositis / dermatomyositis — high CK + skin rash + autoimmune workup.
  • Myasthenia gravis — fluctuating + worse with exertion + diplopia / ptosis.
  • Motor neurone disease — progressive, often asymmetric, fasciculations.

Lab work-up approach

First-line panel: electrolytes (K, Na, Ca, Mg, phosphate), TSH and free T4, vitamin D, CK (creatine kinase), creatinine + eGFR. Add cortisol if Cushing's is suspected; ANA + anti-Jo-1 if inflammatory myopathy is on the differential; acetylcholine receptor antibodies if fluctuating + ocular. Mediora.AI surfaces electrolyte clusters and CK trends; rapid-onset or progressive weakness is a neurological emergency.

Tests Mediora.AI can interpret

Related conditions

When to see a doctor

Acute symmetric weakness with low potassium, calcium or magnesium is treated by replacing the deficit. Chronic proximal weakness with high TSH or low vitamin D usually improves with replacement over 4–8 weeks. CK above 1000 U/L with weakness warrants neurology referral. Rapid-onset (hours-days), asymmetric, or weakness with breathing/swallowing difficulty is a 999/911 emergency — Guillain-Barré, myasthenic crisis, stroke or spinal cord lesion must be excluded urgently. Mediora.AI flags the suggestive lab patterns; do not self-interpret rapid-onset weakness.

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