Kearns-Sayer syndrome: Difference between revisions

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'''Synonyms:''' Kearns Syndrome,  Kearn-Sayre Mitochondrial Cytopathy,  Kearns' Syndrome,  Kearns-Sayre-Shy-Daroff Syndrome
'''Synonyms:''' Kearns Syndrome,  Kearn-Sayre Mitochondrial Cytopathy,  Kearns' Syndrome,  Kearns-Sayre-Shy-Daroff Syndrome


==Overview==
'''Kearns-Sayer syndrome''' is a mitochondrial disorder featuring the triad of: <ref>Adams et al., Principles of Neurology, 6th ed, p984</ref>
'''Kearns-Sayer syndrome''' is a mitochondrial disorder featuring the triad of: <ref>Adams et al., Principles of Neurology, 6th ed, p984</ref>


* chronic progressive external [[ophthalmoplegia]]
* Chronic progressive external [[ophthalmoplegia]]
* [[Cardiomyopathies]] with conduction block
* [[Cardiomyopathy]] with [[heart block]]
* [[Retinitis pigmentosa]]
* [[Retinitis pigmentosa]]


==Diagnosis==
Disease onset is in the first or second decade.  
Disease onset is in the first or second decade.  


* Elevated CSF protein
Diagnostic features include:
* sensorineural deafness  
* Elevated [[CSF]] protein
* [[seizure]]s
* Sensorineural [[deafness]]
* pyramidal signs
* [[Seizure]]s
* [[Pyramidal signs]]
* Ragged-red fibers are found on muscle biopsy.
* Ragged-red fibers are found on muscle biopsy.


 
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[[Category:Genetics]]
[[Category:Genetics]]
[[Category:Cardiology]]
[[Category:Cardiology]]
[[Category:Neurology]]


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Revision as of 09:52, 9 January 2009

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Synonyms: Kearns Syndrome, Kearn-Sayre Mitochondrial Cytopathy, Kearns' Syndrome, Kearns-Sayre-Shy-Daroff Syndrome

Overview

Kearns-Sayer syndrome is a mitochondrial disorder featuring the triad of: [1]

Diagnosis

Disease onset is in the first or second decade.

Diagnostic features include:

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Template:WikiDoc Sources

  1. Adams et al., Principles of Neurology, 6th ed, p984