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Title

KEARNS-SAYRE SYNDROME

Writers

JAVADZADEH MOHSEN

Pages

 Start Page 22 | End Page 23

Abstract

 Introduction KEARNS-SAYRE syndrome (KSS) is specified by pigmentary RETINOPATHY and ophthalmoparesis which should begin before 20 years of age. There are also some other clinical features which are common, some of these freatures are the following: cerebellar ATAXIA, increased cerebrospinal fluid (CSF) protein, conduction block in heart, and proximal myopathy. Many of the patients also have short stature and some of them have multiple endocrinopathies such as diabetes mellitus, hypoparathyroidism, and Addison diseas.

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