Case series uncovers various causes of hypokalemic paralysis, highlighting the need for clinical evaluation to manage complications effectively.
This case series underscores the diverse etiologies of hypokalemic paralysis, spanning endocrine, renal, autoimmune, and genetic causes. A systematic diagnostic approach, guided by clinical and biochemical evaluation, is essential for timely treatment. Identifying the underlying cause not only ensures effective acute management but also prevents recurrence and reduces the risk of serious complications, including cardiac arrhythmias.
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Chaudhary et al. (2025) studied this question.
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