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Ataoglu E. H., Demir B., Tuna M., Cavus B., Cetin F., Temiz L. U., ...More
AMERICAN JOURNAL OF CASE REPORTS, vol.13, pp.187-190, 2012 (ESCI)
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Publication Type:
Article / Article
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Volume:
13
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Publication Date:
2012
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Doi Number:
10.12659/ajcr.883326
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Journal Name:
AMERICAN JOURNAL OF CASE REPORTS
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Journal Indexes:
Emerging Sources Citation Index (ESCI), Scopus
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Page Numbers:
pp.187-190
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Keywords:
Sjogren syndrome, hypopotassemic paralysis, distal renal tubular acidosis
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Istanbul University Affiliated:
No
Abstract
Background: Sjogren syndrome (SS) is an autoimmune-lymphoproliferative disorder characterized by mononuclear cell infiltration of exocrine glands. Clinically, Sjogren syndrome (SS) has a wide spectrum, varying from autoimmune exocrinopathy to systemic involvement. There have been few cases reporting that primary SS developed with distal renal tubular acidosis clinically.