Ehlers-Danlos syndrom (EDS) är en grupp ärftliga sjukdomar. De orsakas av bindvävsförändringar som påverkar leder, hud, blodkärl och inre organ. Överrörlighet i lederna, övertöjbar och mjuk hud samt sköra kärlväggar är vanliga och karaktäristiska symtom.

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Lena Dunham says she is living with Ehlers-Danlos syndrome after she was photographed using a cane. Here are the symptoms of the inherited condition.

Since there's a lot, I'll put it in bullet points: Causes my joints to be  In general a diagnosis of vascular type EDS may provide an opportunity for surveillance Vascular complications in the Ehlers-Danlos syndrome, with special  She's Reddit: A source of statistically significant gendered interest information?1 subreddit, found most questions to be about diagnosis (Derksen, Serlachius, Petrie, & Dalbeth, 2017). In Bullivant, S. & Ruse, M. (eds Aug 2, 2019 hypermobility Ehlers-Danlos syndrome (EDS) is the most common type. Etiology. caused by genetic alterations that affect collagen synthesis  Jun 15, 2017 We had never heard of joint hypermobility or Ehlers-Danlos Syndrome (EDS). We did not know that her symptom descriptions were suggestive of  May 23, 2018 Women are more likely to wait longer for a health diagnosis and to be told it's Men were diagnosed with Ehlers-Danlos syndrome, a group of  Jun 12, 2019 Reddit user u/zebra-eds-warrior described a recent incident where she felt forced to "prove" her Ehlers-Danlos syndrome to use an accessible  Nov 5, 2019 “About 58% of posts to Reddit's r/STD were explicitly requesting a crowd- diagnosis,” said co-author John Ayers, an associate professor in the  Feb 8, 2016 Key features include: joint hypermobility, hyperextensible skin and tissue fragility. · Accurate diagnosis of the type of Ehlers-Danlos syndrome  In: Pizzo PA, Poplack DG,. 2. Page 3.

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Ehlers-Danlos Syndrome, or EDS, is a group of 13 heritable (i.e., genetic) disorders that affect the body’s connective tissues. These tissues—found mostly in the skin, joints, and blood vessel walls—act like a glue to help provide strength and elasticity to the body’s structures, including the digestive system and essential organs. The prognosis of EDS varies greatly depending on the specific type of EDS a patient has. EDS prognosis by disease type. The most common types of EDS (classical, classical-like, and hypermobile) do not greatly affect life expectancy. However, symptoms may become more severe as patients age and joints that have been dislocated multiple times become painful. Click here to subscribe to the Ehlers-Dalos News newsletter.

Ehlers-Danlos Syndrome, or EDS, is a group of 13 heritable (i.e., genetic) disorders that affect the body’s connective tissues.These tissues—found mostly in the skin, joints, and blood vessel walls—act like a glue to help provide strength and elasticity to the body’s structures, including the digestive system and essential organs.

I was recently diagnosed with EDS Hypermobile Type (or type 3, hEDS, etc) Wanted to join and introduce myself. I'm 31, a mom of one 10yo, love video games and cross stitch, and live in the U.S. I've suspected something was "up" with my body since I was about 9 and am so relieved to finally have a diagnosis. I recently went to a rheumatologist, after getting an initial hEDS (type 4) diagnosis.

This morning I was sent a link to a thread on reddit's r/feminism subreddit Angela Janmaat EDS with all the fun associated symptoms. And I'm 

EDS av hypermobilitetstyp (hEDS) är den i särklass vanligaste formen och har ett autosomalt dominant nedärvningsmönster.

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Can somebody please explain what causes it?

I recently went to a rheumatologist, after getting an initial hEDS (type 4) diagnosis. My rheumo ordered a blood panel, X-ray, and echo to rule out other issues. When the results came back he cleared me of any other diagnosis, diagnosed me with a severe vitamin D deficiency, wrote me a script for it, and told me to go back to my PCP. I’m diagnosed with hEDS (received my diagnosis earlier this year after an initial Marfan’s misdiagnosis) but I’m questioning the diagnosis. I don’t doubt that it’s EDS of some kind; however, I do exhibit some criteria that seem to be unusual for hEDS.
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These tissues—found mostly in the skin, joints, and blood vessel walls—act like a glue to help provide strength and elasticity to the body’s structures, including the digestive system and essential organs. The prognosis of EDS varies greatly depending on the specific type of EDS a patient has. EDS prognosis by disease type. The most common types of EDS (classical, classical-like, and hypermobile) do not greatly affect life expectancy.


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Vascular EDS. The diagnosis of vascular EDS (MIM 130050) carries with it the life-threatening risks of blood vessel and organ rupture, sometimes in childhood. The clinical features typical of vascular EDS may be subtle or absent, making diagnosis difficult particularly where there is no positive family history.

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It does not provide medical advice, diagnosis, or treatment. This content is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your physician or 2020-07-01 · After what was likely a long journey, upon diagnosis you learned that you are among the estimated 1 in 5,000 people who have Ehlers-Danlos syndrome (EDS). Although you may be relieved to finally know the cause of your loose joints and other symptoms, you my still need guidance.