Hypoparathyroidism as the First Mani-Festation of Kearns-Sayre Syndrome: A Case Report
محل انتشار: مجله علمی ناباروری ایران، دوره: 5، شماره: 0
سال انتشار: 1393
نوع سند: مقاله ژورنالی
زبان: انگلیسی
مشاهده: 64
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شناسه ملی سند علمی:
JR_IRJN-5-0_003
تاریخ نمایه سازی: 12 شهریور 1402
چکیده مقاله:
Kearns-Sayre syndrome is a mitochondrial myopathy, which was first described by Tomas Kearn in ۱۹۵۸. Diagnostic symptoms of this condition include retinitis pigmentosa, chronic progressive external ophthalmoplegia, and one or more of the following factors: cardiac conduction system diseases, cerebellar ataxia, and cerebrospinal fluid (CSF) with protein content above ۱۰۰ mg/dL. The nature of this uncommon disease is yet to be clarified. According to previous reports, it is uncommon to see hypoparathyroidism as the first manifestation of Kearns-Sayre syndrome. Herein, we report a case of Kearns-Sayre syndrome, with hypoparathyroidism as the first manifestation.
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نویسندگان
Farah Ashrafzadeh
Professor of pediatric neurology, Ghaem Medical Center, Mashhad, Iran
Nosrat Ghaemi
Professor of Pediatric Endocrinology, Imam Reza Center, Mashhad, Iran
Javad Akhondian
Professor of pediatric neurology, Ghaem Medical Center, Mashhad, Iran
Mehran Beiraghi Toosi
Fellowship of Pediatric Neurology, Medical Center, Mashhad, Iran
Saghi Elmi
Pediatrician, Ghaem Medical Center, Mashhad, Iran