Hypokalemic vs. Hyperkalemic periodic paralysis – High Yield NEET PG & INI – CET guide

Hypokalemic vs. Hyperkalemic periodic paralysis – High Yield NEET PG & INI – CET guide

Why This Topic is Important for NEET PG & INI-CET

Periodic paralysis disorders are commonly tested in NEET PG and INI-CET. A solid grasp of hypokalemic and hyperkalemic periodic paralysis will help in answering questions correctly. These conditions involve ion channel activity  affecting muscle function, leading to temporary paralysis. Let’s break it down in a high-yield, exam -focused manner.

What is periodic paralysis?

Periodic paralysis refers to rare neuromuscular disorders characterized by episodes of muscle weakness or paralysis triggered by fluctuation in serum potassium levels.  The two main types are mentioned in the tabular format highlighting key differences.

Mnemonic to remember

“HYPO has HIGH triggers, HYPER has Low Triggers”

  • HYPO Kalemic Paralysis = HIGH Sugar & Carb intake causes an attack .
  • HYPER Kalemic paralysis = LOW Food intake (Fasting) triggers the episode.
Key differences – High – Yield Table
Feature Hypokalemic Periodic ParalysisHyperkalemic Periodic paralysis
Cause Mutation in CACNA1S/SCN4A gene

Primary answer as calcium channel defect

Mutation in SCN4A gene

Primary answer as sodium channel defect

Serum potassium during attack Low (<3.5 mEq/L)High (>5.0 mEq/L)
Triggers High -carb meals, exercise, stressFasting, rest after exercise
Onset Teenage years (10-20 years)Early childhood
Duration of Attack Hours to daysMinutes to hours
Reflexes ReducedNormal
Treatment Potassium supplementation, avoiding triggersGlucose, diuretics (thiazides)

 

Clinical cases to remember

Hypokalemic Periodic Paralysis Hyperkalemic Periodic Paralysis
A 15-year-old male wakes up with sudden muscle weakness after eating a large pizza and soda the previous night

Blood tests show low serum potassium ( 2.5 mEq/L)

A 6-year-old child experiences muscle weakness after skipping breakfast. Symptoms resolve spontaneously after a few hours.

Blood tests show elevated potassium ( 5.6 mEq/L).

 

Diagnosis & Investigations

  • Serum potassium levels during an attack
  • Electromyography (EMG): Shows myotonic discharges in Hyper PP
  • Genetic testing: Confirms mutations in SCN4A (Hyper PP) and CACNA1S/SCN4A (Hypo PP)
  • Exercise Test: Potassium levels drop in Hypo PP and rise in Hyper PP

 

Treatment Approach – High Yield Table

Condition Acute attack Management Long-Term prevention
Hypokalemic PP Oral /IV potassiumAvoid high-carb meals, Acetazolamide
Hyperkalemic PPGlucose + insulin, diureticsLow potassium, diet, acetazolamide

 

Exam Pearls – Must – Know for NEET PG & INI- CET

  • Hypokalemic PP is often linked to thyrotoxic periodic paralysis – commonly seen in Asian populations.
  • Hyperkalemic PP is associated with myotonia (delayed muscle relaxation after contraction).
  • Acetazolamide is used in both conditions as it stabilizes ion channels but can worsen type 2 RTA.

 

📌Related High – Yield Topics to Read click on this link https://www.marwahmedicine.com/blogs/

Suggested reading for doctors sitting for NEET PG and INICET examination from these blog posts

📌Barrter vs. Gitelman syndrome

📌 Renal Tubular Acidosis

📌 Electrolyte disorders – Quick Mnemonics& Cases

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