Talk:Facioscapulohumeral muscular dystrophy/Archive 1

I've
I've begun to expand the basic stub entry for FSHD by copying the basic outline from OCD entry. Please help me expand and complete this entry. Remember to keep entries neutral, fact-based, and to use citations and references. theflyer 14:15, 11 February 2006 (UTC)

Proposed Merge
Ciotog added the merge template on 28 March 2007 suggesting that Facioscapulohumeral dystrophy be merged into this article. These articles are absolutely the same subject and should indeed be merged. Given that the other article is short, has largely duplicate info, and has had little editing (last substantive edit was on 1 Feb 2006), the merge will be simple and straightforward. I will undertake the merge this weekend unless someone disagrees. I will ensure that existing external links and references from the merged article are maintained. Ciotog has already ensured that several of the links are included in this article's infobox. Theflyer 05:54, 29 March 2007 (UTC)
 * Merge complete. Facioscapulohumeral dystrophy now redirects here. Theflyer 15:48, 31 March 2007 (UTC)

FSHD Conference from Boston
On July 16, a large number of researchers and patients gathered in Boston for an FSH Conference. Theflyer 14:47, 18 July 2006 (UTC)

Cleanup and to do
For clean-up and "to do" items, See Talk:Facioscapulohumeral muscular dystrophy/to do. Theflyer 22:33, 8 October 2006 (UTC)
 * Removing the cleanup and to-do template as it results in odd formatting on this talk page (TOC inside the Todo template, section edits not working inside template, etc). The sub-page still exists and the single discussion there can be found at Talk:Facioscapulohumeral muscular dystrophy/to do.  Theflyer 15:50, 31 March 2007 (UTC)

Types
OMIM lists two types of FSHD. The article should have a section or a component of a section that articulates addresses this issue. Theflyer 15:25, 31 March 2007 (UTC)

Is Facioscapulohumeral Muscular Dystrophy Hereditary ??
Is Facioscapulohumeral Muscular Dystrophy Hereditary ??23:11, 25 February 2008 (UTC)69.157.76.64 (talk)
 * Yes, as the Genetics section states, it is Autosomal dominant, which means that only one parent need carry the gene and that there is a 50/50 chance of inherenting the disease. Theflyer (talk) 20:19, 2 March 2008 (UTC)

Review
10.1136/practneurol-2015-001353 JFW &#124; T@lk  11:41, 17 May 2016 (UTC)

External links modified
Hello fellow Wikipedians,

I have just modified 3 external links on Facioscapulohumeral muscular dystrophy. Please take a moment to review my edit. If you have any questions, or need the bot to ignore the links, or the page altogether, please visit this simple FaQ for additional information. I made the following changes:
 * Added archive https://web.archive.org/web/20060306140617/http://www.mda.org/publications/fa-fshd.html to http://www.mda.org/publications/fa-fshd.html
 * Added archive https://web.archive.org/web/20100823233602/http://www.fshsociety.org/pages/resMilestones.html to http://www.fshsociety.org/pages/resMilestones.html
 * Added archive https://web.archive.org/web/20080331074557/http://www.athenadiagnostics.com/content/test-catalog/find-test/service-detail/q/id/57 to http://www.athenadiagnostics.com/content/test-catalog/find-test/service-detail/q/id/57

When you have finished reviewing my changes, you may follow the instructions on the template below to fix any issues with the URLs.

Cheers.— InternetArchiveBot  (Report bug) 11:03, 27 September 2017 (UTC)

aTyr changed directions on clinical study.
This page needs an edit aTyr pharma drug 1940 is not in clinical trials anymore for FSHD. They are now studying ATYR1923, in patients with pulmonary sarcoidosis following acceptance of the Company’s investigational new drug application by the US Food and Drug Administration. https://investors.atyrpharma.com/news-releases/news-release-details/atyr-pharma-announces-initiation-phase-1b2a-study-atyr1923

Thank you. — Preceding unsigned comment added by Debbooksswim (talk • contribs) 17:14, 29 January 2019 (UTC)

Issue with Infobox
I am unable to insert the following text into the symptoms portion of the infobox "Musculoskeletal pain, asymmetric muscle weakness, winged scapula"

It gives me the error "Warning: Page using Template:Infobox medical condition with unknown parameter "symptoms     " (this message is shown only in preview)."

It worked after the first few previews, but it seemed to 'break' after I tried inserting a citation.

Anyone know how to fix? Lukelahood (talk) 15:51, 12 February 2020 (UTC)

Figured it out. There was a unrecognizable space character where a space normally is, in the code. Lukelahood (talk) 15:35, 9 March 2020 (UTC)