Talk:Childhood absence epilepsy

Wiki Education Foundation-supported course assignment

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  This article was the subject of a Wiki Education Foundation-supported course assignment, between 29 June 2020 and 21 August 2020. Further details are available on the course page. Student editor(s): AHean2022, LLu, Future UCSF Pharm.D., K. Lam, Future UCSF Pharm.D..

Above undated message substituted from Template:Dashboard.wikiedu.org assignment by PrimeBOT (talk) 17:26, 16 January 2022 (UTC)Reply

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Would the monitor of this page mind if I edited it to include the clinical and EEG characteristics of this disease to the foreground and the genetics within the proper context?

Karmattol (talk) 18:54, 11 November 2008 (UTC)Reply

Well, there isn't any particular monitor for this (or any other) page so go ahead and edit whatever you like (that includes the Juvenile Myoclonic Epilepsy page). I'm not a clinician so I left a lot of the EEG stuff out of these pages when I created them. --Dpryan (talk) 19:51, 11 November 2008 (UTC)Reply
Please do what you can to expand this. IMO, the detailed table of mutations is not appropriate for Wikipedia or its intended audience. In addition, they are likely to become out-of-date very quickly, which is why we have online databases to collect such things. WP:MEDMOS has some advice for writing about diseases. Colin°Talk 21:01, 11 November 2008 (UTC)Reply