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Perry syndrome: Difference between revisions
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a disorder characterised by clinical signs of parkinsonism, depression/apathy, weight loss, respiratory symptoms, mutations in the DCTN1 gene and TAR DNA-binding protein 43 (TDP-43) pathology | Perry syndrome is a disorder characterised by clinical signs of [[parkinsonism]], depression/apathy, weight loss, respiratory symptoms, mutations in the [[dynein|DCTN1 gene]] and TAR DNA-binding protein 43 (TDP-43) pathology | ||
<ref>[https://jnnp.bmj.com/content/89/5/482 Establishing diagnostic criteria for Perry syndrome]</ref> | <ref>[https://jnnp.bmj.com/content/89/5/482 Establishing diagnostic criteria for Perry syndrome]</ref> | ||
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Revision as of 22:16, 10 January 2019
Perry syndrome is a disorder characterised by clinical signs of parkinsonism, depression/apathy, weight loss, respiratory symptoms, mutations in the DCTN1 gene and TAR DNA-binding protein 43 (TDP-43) pathology