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، جلد ۹، شماره ۴، صفحات ۱۸۶-۱۹۱
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| عنوان فارسی |
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| چکیده فارسی مقاله |
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| کلیدواژه‌های فارسی مقاله |
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| عنوان انگلیسی |
Kearns Sayre Syndrome: A Rare Cause of Mitochondrial Diabetes and Hypogonadotropic Hypogonadism |
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| چکیده انگلیسی مقاله |
Kearns-Sayre syndrome is a rare mitochondrial disease that presents before the age of 20 years with ptosis, external ophthalmoplegia, and pigmentary retinopathy associated with endocrine and cardiac conduction abnormalities. Here we report an 18-year-old female presenting with fever, cough, secondary amenorrhea, diabetes ptosis, external ophthalmople gia, and ataxia . Fundosc opy revealed pigmen tary retinopathy. ECG showed intraventricular conduction abnormalities, and 2D echocardiography revealed global left ventricular hypokinesia with reduced ejection fraction. Hence, the diagnosis of Kearns-Sayre syndrome was made. |
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| کلیدواژه‌های انگلیسی مقاله |
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| نویسندگان مقاله |
| Sriram Mudraje
Department of Endocrinology, People’s College of Medical Sciences and Research Centre, Bhopal,India.
| Jaideep Khare
Department of Endocrinology, People’s College of Medical Sciences and Research Centre, Bhopal,India.
| Nancy Garg
Department of Endocrinology, People’s College of Medical Sciences and Research Centre, Bhopal,India.
| Sushil Jindal
Department of Endocrinology, People’s College of Medical Sciences and Research Centre, Bhopal,India.
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| نشانی اینترنتی |
https://crcp.tums.ac.ir/index.php/crcp/article/view/1010 |
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