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Perry syndrome: Difference between revisions
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<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> | ||
{{disease|Perry|Q99}} | |||
==Links== | ==Links== | ||
[https://karmel.miraheze.org/w/index.php?title=S%C3%ADndrome_de_Perry&oldid=6596 Karmel:Síndrome de Perry] | [https://karmel.miraheze.org/w/index.php?title=S%C3%ADndrome_de_Perry&oldid=6596 Karmel:Síndrome de Perry] | ||
<references/> | <references/> | ||
Revision as of 22:46, 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
Disease classification WHO
Perry Q99