2018•University journal of medicine and medical specialitiesRequires access

Recurrent Hypokalemic Paralysis - An Interesting Cause

Devan

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Abstract

Abstract : Recurrent hypokalemic paralysis is caused  y either channelopathies or by conditions associated with            recurrent or persistent renal or non renal losses of potassium. Distal renal tubular acidosis (dRTA) is one of the causes of renal potassium loss leading to hyokalemia. One of the                important presentations of dRTA is recurrent hypokalemic weakness, which can be life threatening.a We would like to present one such case of recurrent hypokalemic paralysis with respiratory weakness secondary to dRTA. Type 1 or dRTA involves impaired distal acidification of urine. dRTA often presents as renal stone disease with nephrocalcinosis in adults, rickets and growth retardation in children with              ultimate short stature in adulthood. Our case is a 19-year-old male who had features of dRTA like recurrent hypokalemic paralysis, metabolic acidosis, stunted growth, rickets and nephrocalcinosis. Keyword :Recurrent hypokalemic paralysis, Metabolic              acidosis, Abnormal urine pH, Short stature,Rickets,               Nephrocalcinosis, Distal Renal Tubular Acidosis.

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Abstract : Recurrent hypokalemic paralysis is caused  y either channelopathies or by conditions associated with            recurrent or persistent renal or non renal losses of potassium. Distal renal tubular acidosis (dRTA) is one of the causes of renal potassium loss leading to hyokalemia. One of the                important presentations of dRTA is recurrent hypokalemic weakness, which can be life threatening.a We would like to present one such case of recurrent hypokalemic paralysis with respiratory weakness secondary to dRTA. Type 1 or dRTA involves impaired distal acidification of urine. dRTA often presents as renal stone disease with nephrocalcinosis in adults, rickets and growth retardation in children with              ultimate short stature in adulthood. Our case is a 19-year-old male who had features of dRTA like recurrent hypokalemic paralysis, metabolic acidosis, stunted growth, rickets and nephrocalcinosis. Keyword :Recurrent hypokalemic paralysis, Metabolic              acidosis, Abnormal urine pH, Short stature,Rickets,               Nephrocalcinosis, Distal Renal Tubular Acidosis.

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Available abstract

Abstract : Recurrent hypokalemic paralysis is caused  y either channelopathies or by conditions associated with            recurrent or persistent renal or non renal losses of potassium. Distal renal tubular acidosis (dRTA) is one of the causes of renal potassium loss leading to hyokalemia. One of the                important presentations of dRTA is recurrent hypokalemic weakness, which can be life threatening.a We would like to present one such case of recurrent hypokalemic paralysis with respiratory weakness secondary to dRTA. Type 1 or dRTA involves impaired distal acidification of urine. dRTA often presents as renal stone disease with nephrocalcinosis in adults, rickets and growth retardation in children with              ultimate short stature in adulthood. Our case is a 19-year-old male who had features of dRTA like recurrent hypokalemic paralysis, metabolic acidosis, stunted growth, rickets and nephrocalcinosis. Keyword :Recurrent hypokalemic paralysis, Metabolic              acidosis, Abnormal urine pH, Short stature,Rickets,               Nephrocalcinosis, Distal Renal Tubular Acidosis.

Key concepts: Distal renal tubular acidosis, Nephrocalcinosis, Renal tubular acidosis, Medicine, Short stature, Hypokalemia, Rickets, Hypokalemic periodic paralysis

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