The Challenges of Living with a Rare Type of EDS - Dr. Serwet Demirdas

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  • Опубліковано 16 вер 2024

КОМЕНТАРІ • 4

  • @vanessabuchanan4691
    @vanessabuchanan4691 11 місяців тому

    I have a rare polymorphic mutation in Aebp1 associated with classic type 2 subtype and Aortic Aneurysm only seen once before. I also have a rare ZNF469 mutation seen in Brittle Cornea never seen before. It is likely to be disruptive.

  • @shannongreenwell1278
    @shannongreenwell1278 11 місяців тому +1

    I have EDS/ Classical subtype. It took me turning 48 years of age to learn about it. I got Dx by my Neurologist. My biggest challenge is pain and subluxation and Migraines, Dysautonomia.

    • @tes-sr6zh
      @tes-sr6zh 11 місяців тому +1

      ​@@sharonkaysummerford2099 why in the world are you being given Tylenol of all the drugs out there? Your kidneys hun