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Hypoparathyroidism as the first manifestation of kearns-sayre syndrome: a case report.

Authors :
Ashrafzadeh F
Ghaemi N
Akhondian J
Beiraghi Toosi M
Elmi S
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