Wikisage, the free encyclopedia of the second generation and digital heritage, wishes you merry holidays and a happy new year!
Perry syndrome: Difference between revisions
Jump to navigation
Jump to search
mNo edit summary |
No edit summary |
||
(4 intermediate revisions by the same user not shown) | |||
Line 1: | Line 1: | ||
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 ||[[File:Under construction icon.png |32px ]]<ref>https://omim.org/entry/168605?search=Perry&highlight=perry</ref>|G80}} | |||
==Links== | |||
[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