HYPOPARATHYROIDISM AS THE FIRST MANIFESTATION OF KEARNS-SAYRE SYNDROME: A CASE REPORT

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ASHRAFZADEH FARAH; GHAEMI NOSRAT; AKHONDIAN JAVAD; BEIRAGHI TOOSI MEHRAN; ELMI SAGHI

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Journal: Iranian Journal of Child Neurology Year:2013 | Volume:7 | Issue:4 Page(s): 53-57

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Title

HYPOPARATHYROIDISM AS THE FIRST MANIFESTATION OF KEARNS-SAYRE SYNDROME: A CASE REPORT

Author(s)

Keywords

KEARNS-SAYRE

HYPOPARATHYROIDISM

OPHTHALMOPLEGIA

MITOCHONDRIAL CYTOPATHY

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.

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APA: Copy

ASHRAFZADEH, FARAH, GHAEMI, NOSRAT, AKHONDIAN, JAVAD, BEIRAGHI TOOSI, MEHRAN, & ELMI, SAGHI. (2013). HYPOPARATHYROIDISM AS THE FIRST MANIFESTATION OF KEARNS-SAYRE SYNDROME: A CASE REPORT. IRANIAN JOURNAL OF CHILD NEUROLOGY (IJCN), 7(4), 53-57. SID. https://sid.ir/paper/303393/en

Vancouver: Copy

ASHRAFZADEH FARAH, GHAEMI NOSRAT, AKHONDIAN JAVAD, BEIRAGHI TOOSI MEHRAN, ELMI SAGHI. HYPOPARATHYROIDISM AS THE FIRST MANIFESTATION OF KEARNS-SAYRE SYNDROME: A CASE REPORT. IRANIAN JOURNAL OF CHILD NEUROLOGY (IJCN)[Internet]. 2013;7(4):53-57. Available from: https://sid.ir/paper/303393/en

IEEE: Copy

FARAH ASHRAFZADEH, NOSRAT GHAEMI, JAVAD AKHONDIAN, MEHRAN BEIRAGHI TOOSI, and SAGHI ELMI, “HYPOPARATHYROIDISM AS THE FIRST MANIFESTATION OF KEARNS-SAYRE SYNDROME: A CASE REPORT,” IRANIAN JOURNAL OF CHILD NEUROLOGY (IJCN), vol. 7, no. 4, pp. 53–57, 2013, [Online]. Available: https://sid.ir/paper/303393/en

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