Talk:Ohtahara syndrome
Jump to navigation
Jump to search
 | This article is rated Start-class on Wikipedia's content assessment scale. It is of interest to the following WikiProjects: | |||||||||||||
| ||||||||||||||
 | Ideal sources for Wikipedia's health content are defined in the guideline Wikipedia:Identifying reliable sources (medicine) and are typically review articles. Here are links to possibly useful sources of information about Ohtahara syndrome.
|
Who was Ohtahara?
I'm assuming (from the name and medical nomenclature conventions) that he was (1) Japanese, at least by descent and (2) the researcher who first described the syndrome, but what was his full name, where was he working, and when did he do the formal description? All of this is interesting and encyclopedic information that deserves to be in the article, if it can be found. Lockesdonkey (talk) 19:55, 4 July 2010 (UTC)
- This might help:http://books.google.fr/books?id=eocv90bllDEC&lpg=PR14&ots=Q6YVo1IrE7&dq=%C3%89pilepsies%20avec%20suppression%20Burst&pg=PR14#v=onepage&q=ohtahara&f=false— Preceding unsigned comment added by Palpalpalpal (talk • contribs) 09:37, 30 March 2011 (UTC)
Why is there an inheritance pattern?
There is no single or group of genes labelled responsible for the disease and it is equally found in girls and boys (therefore NOT x-linked recessive). — Preceding unsigned comment added by 170.223.207.6 (talk) 23:15, 28 February 2018 (UTC)