Journal of Clinical and Biomedical Sciences
Year: 2019, Volume: 9, Issue: 3, Pages: 81-83
Case Report
Rumaisa Ahmed1*, Prasanna Kumar2, Tameem Imran3
1. Junior Resident, Department Of Medicine, Sri Devaraj Urs Medical College, Sri Devaraj Urs Academy of Higher Education and Research, Kolar
2. Assistant professor, Department Of Medicine, Sri Devaraj Urs Medical College, Sri Devaraj Urs Academy of Higher Education and Research, Kolar
3. Senior Resident, Department Of Medicine, Sri Devaraj Urs Medical College, Sri Devaraj Urs Academy of Higher Education and Research, Kolar
*Corresponding Author
E-mail: [email protected]
Mobile No : 9482216030
Sjogren's syndrome is a slowly progressing autoimmune disease that is characterized by lymphocytic infiltra-tion of the exocrine glands resulting in impaired secretory function. There are varied causes of quadriparesis ranging from cervical cord myelopathy to neuromuscular junction disorders. Even though hypokalemia is a fre-quent cause of quadriparesis but is usually due to periodic paralysis. Here we present a case in which hypokale-mia secondary to Sjogren’s syndrome presented with quadriparesis, which progressed, to respiratory paralysis.
Keywords: Sjogren's syndrome, distal renal tubular acidosis, hypokalemia, peripheral vascular disease
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