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Perry syndrome: Difference between revisions
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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 | [[Thomas L.Perry|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> | ||
{{disease|Perry|G80}} | {{disease|Perry ||[[File:Under construction icon.png |32px ]]<ref>https://omim.org/entry/168605?search=Perry&highlight=perry</ref>|G80}} | ||
==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/> | ||
Latest revision as of 22:55, 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
