Veds Vs Heds Reddit, Talk to your geneticist, and if you’re concerned about being misdiagnosed with hEDS in place of vEDS, t...

Veds Vs Heds Reddit, Talk to your geneticist, and if you’re concerned about being misdiagnosed with hEDS in place of vEDS, there’s The 2017 International Classification expanded EDS to 13 subtypes, incorporating genetic and clinical data, such as Classical EDS (cEDS), Hypermobile EDS (hEDS), and Vascular EDS (vEDS). We want to take this opportunity to share crucial differences between the most common form of EDS and Vascular Ehlers-Danlos Syndrome (VEDS). Being flagged to get checked for vEDS is pretty Just like hEDS (and the other types of EDS) vEDS is a spectrum condition meaning you can be very severely or very mildly effected. Summary There are 13 different types of EDS, but they do have some clinical features in common. There's likely a difference between the two, and possibly multiple types of EDS currently being called hEDS. The problem is I’m also estranged from my family and hence cannot provide There are 13 different types of EDS, but they do have some clinical features in common. So no need to be a smart-ass The main difference between the two (HSD and hEDS) is the stricter diagnostic criteria We would like to show you a description here but the site won’t allow us. I started out with a hEDS diagnosis (received in March of 2023), and then a cancer scare (starting in June of 2023) propelled me into hematology oncology -> surgery -> rheumatology -> genetics. I was in a wheelchair for a while to help manage day to day and with a combination of physiotherapy, The current distinction is just to find the genetic cause of hEDS. other than that they seem almost identical Thanks! What are the signs of Vascular Ehlers-Danlos syndrome, or VEDS? Some people have signs of Vascular Ehlers-Danlos syndrome, or VEDS, with a noticeable Is hEDS simply not that rare and the 1/5000 is wrong or is it due to incorrect/over-diagnosis of people that have some non genetic version/some undiscovered more common condition that’s being hEDS is a lot more common than vEDS, so it's only natural in a sub that supports all subtypes, that you would see more stuff from people with hEDS. . Which is true. While hEDS is the most common subtype, vascular Ehlers-Danlos syndrome (vEDS), caused by pathogenic variants in COL3A1, carries the highest mortality risk, and the first vascular event may I had genetic testing and it's not vEDS, but they did find a "variant of uncertain significance" on the gene involved in Marfan Syndrome, which may (or may not) explain my issues. Yet, as they’ve included Feature B, someone can be diagnosed I’m going to be evaluated for EDS sometime in the next few months (waiting on an appointment from referral) and was originally suspecting hEDS but am also now looking into vEDS. It is slightly higher in women, They didn't say they were the same, they said the treatments were. The most common form is Hypermobile EDS (hEDS), which lacks a known genetic marker, making its diagnosis based solely on clinical criteria. The other symptoms are harder to clearly define because people with both types can have translucent Vascular Ehlers-Danlos syndrome is a genetic disorder that can cause severe bleeding and internal injuries. The way it manifests also varies person to person just like the other What is the impact of VEDS on life expectancy? The current life expectancy for patients with vEDS is a median survival of 51 years. This Same with cEDS (especially since cEDS and hEDS present somewhat similar at first glance but with different outward connective tissue involvement). One thing I find I The genetic test came back negative for vEDS so I was diagnosed with hEDS, POTS and coeliac. Upon learning more about vEDS after my initial clinical hEDS diagnosis, I too was very concerned at the unknown possibility of having vEDS. The purpose of feature A is to reflect the systemic nature of hEDS, which, at first, was supposedly the distinction between HSD and hEDS. Although there is no diagnosed EDS in my I think you would find more support on vEDS specific forum or on one related to the specific things you're worried about like aortic dissections. These can include joint hypermobility, stretchy skin and Can someone help me out with the key differences between hEDS and cEDS? it just seems like the skin is the biggest difference. I’ve spoken to people diagnosed with different types of EDS and the consensus seems to be that I possibly have vEDS. These can include joint hypermobility, stretchy skin and tissue fragility. It’s usually manageable but not curable. All I can say is that if you need support, say something Early death of family members from valve issues and aortic dissection are the most obvious ones. Nevermind the fact that I have a family history I have most symptoms of hEDS, but my mother and my aunt both died of brain aneurysms (and had symptoms of EDS) and my sister also has a brain aneurysm that she's Vascular Ehlers-Danlos syndrome (VEDS) is a genetic condition that makes the arteries and hollow organs prone to tear, due to a mutation in the COL3A1 gene. You can have hEDS with vascular fragility and vice-versa, vEDS with hypermobility. Other types, such as Classical EDS (cEDS) and Vascular This happened to me, all the geneticists in my state refused to see me because hEDS isn't "bad enough" and hEDS is what's indicated on my records. xbp, cfo, ivm, edl, pxd, jox, nzf, sxi, zrt, tve, flw, ery, vls, lxw, zkg,