Talk:Limb–girdle muscular dystrophy/Archive 1

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Contradicting information[edit]

The page states: "Common symptoms of limb-girdle muscular dystrophy are muscle weakness, myoglobinuria, pain, myotonia, cardiomyopathy, elevated serum CK, and rippling muscles."

And only a bit further:

"Generally pain is not present with LGMD, and mental function is not affected."

So, is pain typical, or not?

DiamonDie (talk) 16:14, 11 November 2008 (UTC)[reply]

LGMD subtype changes[edit]

Good morning, Wikipedians! There have been some changes to the LGMD subtype nomenclature system.

  • Renaming: The subtypes of LGMD were renamed as LGMD +R, if recessive, and D if dominant + gene-related. For example, LGMD2J (autosomal recessive) was renamed as "LGMD R10 titin-related".
  • Removal: Some subtypes of LGMD were removed and were reclassified. For example, LGMD1A has been reclassified as "myofibillar myopathy".
  • Additions: Some new subtypes have been added (e.g. Bethlem myopathy recessive, which is LGMD R22 Collagen-6 related).

[1] As I am not a doctor, please review this information in a medical perspective. Thank you so much! Poeticfeelings (talk) 10:45, 6 August 2019 (UTC)[reply]

will look--Ozzie10aaaa (talk) 14:23, 6 August 2019 (UTC)[reply]

References

  1. ^ Straub V, Murphy A, Udd B; LGMD workshop study group. 229th ENMC international workshop: Limb girdle muscular dystrophies - Nomenclature and reformed classification Naarden, the Netherlands, 17-19 March 2017. Neuromuscul Disord. 2018 Aug;28(8):702-710. doi: 10.1016/j.nmd.2018.05.007. Epub 2018 May 24.

Homeopathic treatment[edit]

Hi Gerryharrington, it is my opinion that the information you provided is not useful to readers in its present form, for the following reasons:

  1. The article you cited is not a medical reference, despite the content being medical information
  2. This is anecdotal evidence, not even at the level of a case report, and even case reports are not usually suitable for wikipedia
  3. The article does not specify the type of LGMD, and considering that none of the subtypes are closely related on a molecular level, a treatment that works for one subtype is likely not translatable to another subtype.
  4. The article does not specify the treatment. The only way to pursue it is by visiting the same doctor in India. Seeing another homeopathic doctor seems to be unlikely to be successful as they would not know the same treatment (unless it is published elsewhere, in which case you should cite that article).

Please let me know your thoughts.— Preceding unsigned comment added by Lukelahood (talkcontribs) time, day month year (UTC)

I agree w/ Lukelahood--Ozzie10aaaa (talk) 12:37, 24 October 2021 (UTC)[reply]
I also agree and have removed the problematic passage again. — kashmīrī TALK 13:20, 24 October 2021 (UTC)[reply]