Hypoparathyroidism as the First Manifestation of Kearns-Sayre Syndrome: A Case Report

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 atax...

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Autores principales: ASHRAFZADEH, Farah, GHAEMI, Nosrat, AKHONDIAN, Javad, BEIRAGHI TOOSI, Mehran, ELMI, Saghi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Shahid Beheshti University of Medical Sciences 2013
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3943048/
https://www.ncbi.nlm.nih.gov/pubmed/24665319
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author ASHRAFZADEH, Farah
GHAEMI, Nosrat
AKHONDIAN, Javad
BEIRAGHI TOOSI, Mehran
ELMI, Saghi
author_facet ASHRAFZADEH, Farah
GHAEMI, Nosrat
AKHONDIAN, Javad
BEIRAGHI TOOSI, Mehran
ELMI, Saghi
author_sort ASHRAFZADEH, Farah
collection PubMed
description 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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spelling pubmed-39430482014-03-24 Hypoparathyroidism as the First Manifestation of Kearns-Sayre Syndrome: A Case Report ASHRAFZADEH, Farah GHAEMI, Nosrat AKHONDIAN, Javad BEIRAGHI TOOSI, Mehran ELMI, Saghi Iran J Child Neurol Case Report 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. Shahid Beheshti University of Medical Sciences 2013 /pmc/articles/PMC3943048/ /pubmed/24665319 Text en © 2013: Iranian Journal of Child Neurology This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
ASHRAFZADEH, Farah
GHAEMI, Nosrat
AKHONDIAN, Javad
BEIRAGHI TOOSI, Mehran
ELMI, Saghi
Hypoparathyroidism as the First Manifestation of Kearns-Sayre Syndrome: A Case Report
title Hypoparathyroidism as the First Manifestation of Kearns-Sayre Syndrome: A Case Report
title_full Hypoparathyroidism as the First Manifestation of Kearns-Sayre Syndrome: A Case Report
title_fullStr Hypoparathyroidism as the First Manifestation of Kearns-Sayre Syndrome: A Case Report
title_full_unstemmed Hypoparathyroidism as the First Manifestation of Kearns-Sayre Syndrome: A Case Report
title_short Hypoparathyroidism as the First Manifestation of Kearns-Sayre Syndrome: A Case Report
title_sort hypoparathyroidism as the first manifestation of kearns-sayre syndrome: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3943048/
https://www.ncbi.nlm.nih.gov/pubmed/24665319
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