An Unusual Initial Presentation of Sjögren’s Syndrome: Severe Hypokalemic Paralysis Secondary to Distal Renal Tubular Acidosis
Author(s) -
Erkan Şengül,
Fatih Bunul,
Ayten Yazıcı,
Aysun Şengül,
Sevim Dindar,
Gokcen Selma Kilic Halhalli,
Emine Binnetoğlu
Publication year - 2013
Publication title -
eurasian journal of medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.337
H-Index - 13
eISSN - 1308-8742
pISSN - 1308-8734
DOI - 10.5152/eajm.2013.43
Subject(s) - distal renal tubular acidosis , medicine , hypokalemia , renal tubular acidosis , sjögren syndrome , hypokalemic periodic paralysis , gastroenterology , dermatology , acidosis , systemic disease , disease
Sjögren's syndrome is mainly affects the exocrine glands. Patients usually complain of persistent dryness of the mouth and eyes. However, nonexocrine organs such as the kidneys are often affected in these patients. Distal renal tubular acidosis (dRTA) and interstitiel nephritis are common in Sjögren's syndrome. Nonetheless, severe hypokalemia and paralysis secondary to dRTA are unusual initial manifestation of Sjögren's syndrome. Here, we describe a case of a 48 year old women admitted to the emergency setting with severe hypokalemic paralysis and diagnosed Sjögren's syndrome.
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