Article Text
Neurology and Developmental Paediatrics
PO-0823 Hypoparathyroidism As The First Manifestation Of Kearns-sayre Syndrome: A Case Report
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.
- Kearns-Sayre
- Hypoparathyroidism
- Ophthalmoplegia
- Mitochondrial cytopathy