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Hypoparathyroidism as the first manifestation of kearns-sayre syndrome: a case report.
- Source :
-
Iranian journal of child neurology [Iran J Child Neurol] 2013 Fall; Vol. 7 (4), pp. 53-7. - Publication Year :
- 2013
-
Abstract
- Objective: Kearns-Sayre syndrome is a mitochondrial myopathy, which was first described by Tomas Kearn in 1958. Diagnostic symptoms include retinitis pigmentosa, chronic and progressive external ophthalmoplegia plus one or more of following factors: heart conduction system disorders, cerebellar ataxia, or cerebrospinal fluid (CSF) protein content above 100 mg/dL. The nature of this uncommon disease is yet to be clarified. In this paper, we report a case of Kearns-Sayre syndrome. According to the previous records, the first manifestation of Kearns- Sayre syndrome as hypoparathyroidism is uncommon and in this article, we report a case with this problem.
Details
- Language :
- English
- ISSN :
- 1735-4668
- Volume :
- 7
- Issue :
- 4
- Database :
- MEDLINE
- Journal :
- Iranian journal of child neurology
- Publication Type :
- Report
- Accession number :
- 24665319