Veds vs heds.
The Types of EDS There are several forms of EDS.
Veds vs heds Joints move beyond the normal range, causing frequent dislocations and subluxations. 6 at 12:00 pm ET. Find out how hEDS is diagnosed and can be managed. 3 days ago · Red Dead Redemption is already available on Switch and has been for quite some time, but soon Switch 2 owners will get to enjoy an enhanced edition of the game. Keeping my fingers crossed for you! Hypermobile EDS (hEDS): The most common subtype, hEDS, is now thought to affect approximately 1 in 500 to 1 in 5,000 individuals based on newer studies. Results The AI classifier showed excellent performance with as few as 13 vEDS training images and distinguished vEDS from both controls and individuals with hEDS with high accuracy, achieving an area under the receiver operating characteristic curve ≥ 0. I have severe POTS, mitral valve prolapse, heel papules, possibly sunken chest, claw toes, joint pain, hyper mobility in my fingers and probably generalized hypermobility as well. Mar 25, 2025 · DAYTON − Reds prospects sent the organization's big-leaguers into the MLB regular season on a slightly sour note. Easy bruising is also common in most EDS types and for other reasons. Other than that the clinical signs are pretty unreliable and the only way to know is genetic testing. Jul 23, 2025 · Reds vs. Symptoms range across a wide spectrum and include joint hypermobility, stretchy and “velvety” skin, chronic pain in the bones and muscles, osteoporosis, osteoarthritis, gastrointestinal What should I know about hypermobile Ehlers-Danlos Syndrome (hEDS) and pregnancy? hEDS pregnancies are generally favorable but may involve challenges like pelvic girdle pain, joint dislocations, and a higher risk of pelvic organ prolapse postpartum. According to researchers, fewer delays in diagnosing their disease — “the diagnosis delay is 9 years [longer] in hEDS than in” the more severe disorders — appear to aid people with vEDS and LDS to develop better coping abilities. So skin seems normal in the early stages of hEDS. conducted one of the most detailed examinations of inflammatory biomarkers in vEDS. Fatigue and These distinct facial differences between vEDS and hEDS highlight the variable presentation of EDS subtypes, with vEDS having a more recognizable facial profile that aids in early suspicion, while hEDS requires a more symptom-focused approach due to its lack of consistent facial markers. The Red Raiders are 13. Vascular EDS and Systemic Inflammation Though genetically distinct from hEDS, vascular EDS (vEDS) offers additional insight into the role of inflammation in EDS more broadly. Vascular EDS (vEDS) A rare and severe form affecting blood vessels, with a higher risk of organ rupture. A study, published in November 2019, looked at Overview of Life Expectancy with EDS Life expectancy in Ehlers-Danlos Syndrome (EDS) varies significantly depending on the specific subtype. Oct 21, 2024 · Vascular Ehlers-Danlos Syndrome (VEDS) is a lethal condition – often misunderstood because it’s named within the Ehlers-Danlos family of conditions that do not generally pose significantly elevated risk of sudden death. The affected genes in vEDS are COL3A1 affecting Type III collagen and COL1A1 affecting Type 1 collagen (MIM 130050) 50% of patients diagnosed with vEDS have a de novo mutation (ie, neither parent is affected). The exact genetic cause is yet to be identified. I decided to meet with a rheumatologist and he wants to do genetic testing first, to exclude other types. 2nd, 2025, and now you can see just how it measures up to the Switch version in the video above. [1] These may be noticed at birth or in early childhood. Vascular Ehlers–Danlos syndrome (vEDS) The inheritance pattern of vEDS is autosomal dominant. Proper Apr 10, 2022 · Vascular Ehlers-Danlos syndrome is a genetic disorder that can cause severe bleeding and internal injuries. Local Interpretable Model-agnostic Explanations highlighted facial regions already established to characterize the facial features of vEDS 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. Our findings indicate that these cells share a deregulated expression of many matrix-related genes and a widespread disarray of several ECM structural constituents, thus highlighting the functional You can have hEDS with vascular fragility and vice-versa, vEDS with hypermobility. But then again, they had no business losing either. Throwaway account. . Earlier estimates suggested it was much rarer, but increasing awareness and improved diagnostic criteria have led to more diagnoses. 18 matchup between the Detroit Red Wings and Seattle Kraken with betting odds over/under, game spread, moneyline, prediction, TV channel and more. Talk to your geneticist, and if you’re concerned about being misdiagnosed with hEDS in place of vEDS, there’s genetic testing to rule out vEDS. VEDS is caused by a mutation in the gene that makes collagen III in the body. vEDS is caused by mutations in the COL3A1 gene. I will say that these are incredibly nonspecific -- it's possible to have everything mentioned above and still end up with a hEDS diagnosis. Its estimated prevalence is between one in 5,000 and one in 20,000 people worldwide. Do hEDS symptoms also affect people with vEDS and vice versa? Schematic illustration summarizing the processes likely involved in the pathogenesis of cEDS, vEDS, and hEDS/HSD derived from transcriptome and in vitro studies of patients’ skin fibroblasts. In 2017, an International Classification aimed to provide clarity to health professionals, patients, and researchers emphasizing the distinction of vascular complications hEDS patients frequently experience joint dislocations, chronic musculoskeletal pain, and gastrointestinal disorders like irritable bowel syndrome (IBS) and gastroesophageal reflux disease (GERD). This condition is typically caused by mutations in the COL3A1 hEDS is mainly identified by generalized joint hypermobility (GJH), additional joint issues, and obvious skin signs, which are less severe than those seen in Classic EDS (cEDS) or Vascular EDS (vEDS). These can include joint hypermobility, stretchy skin and tissue fragility. Nationals prediction, odds, line, start time: 2025 MLB picks, best bets for July 23 by proven model SportsLine's model simulated Washington Nationals vs. hEDS requires a combination of generalized joint hypermobility, specific clinical features, and exclusion of other conditions. Vascular Ehlers-Danlos Syndrome (vEDS, previously Ehlers-Danlos Type IV) is a rare genetic disorder with an estimated prevalence of 1/50,000 to 1/200,000 (1). [7] Symptoms often include loose joints, joint pain, stretchy, velvety skin, and abnormal scar formation. Jun 30, 2025 · Garrett Crochet's strikeout ability highlights our Reds vs. Rockstar recently confirmed that Red Dead Redemption is getting a Switch 2 release on Dec. The official scoreboard of the Cincinnati Reds including Gameday, video, highlights and box score. [1][4] The existing 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 characteristic appearance, while others do not have any outward signs of the condition. But, in hEDS (Hypermobile Ehlers Danlos Syndrome), you have only a minimal amount of elastic skin. It’s usually manageable but not curable. Local Interpretable Model-agnostic Explanations highlighted facial regions already established to characterize the facial features of Through 162 Reds and Roto-Rooter Unclogging the Bases Reds Movement that Inspires pres. Diagnostic Criteria: hEDS vs. Unlike other EDS subtypes primarily characterized by joint hypermobility and skin elasticity, vEDS is distinguished by its impact on the vascular system, posing a significant risk of life-threatening complications. Half had to be removed and healed well. I have not been tested yet. Kyphoscoliotic EDS (kEDS) Oct 28, 2020 · What is hEDS? hEDS, which was also known as EDS type 3 or EDS-hypermobile type (EDS-HT), is the most common form of EDS. I'm thinking if hEDS or cEDS fits better (or even clEDS)? I'm experienced sigmoid volvulus on night and my colon ended up perforating. Mar 14, 2025 · I got diagnosed with POTS over a year ago. Individuals with vEDS are at high risk for spontaneous rupture of blood vessels, intestines, or other organs, often without prior warning. However, I am extremely poor and I am wondering if it is worth it. vEDS BASICS Learn the basics about vascular EDS What is vascular EDS? Learn about the most frequently asked questions View More Vascular Ehlers-Danlos syndrome (VEDS) is one of the different subtypes of Ehlers-Danlos syndrome (EDS). I (20f) have been advised to get tested for EDS. Apparently my Jul 23, 2025 · Game summary of the Cincinnati Reds vs. The median life expectancy is 50 years. Sometimes patients with hEDS will suspect that they may have a rare form of EDS such as vascular EDS. Tyler Glasnow had his shakiest outing since returning from the 60-day IL, allowing four Vascular Ehlers Danlos syndrome, or VEDS, is caused by changes in the gene called COL3A1 that tells the body how to make collagen III. When you receive a new diagnosis, this can be a time of great stress, anxiety and confusion. 1 day ago · Boston Bruins vs Detroit Red Wings odds, picks, prediction, and betting preview for their NHL matchup on Tuesday, December 2. Vascular EDS (vEDS): Associated with COL3A1 mutations, defined by arterial rupture risk, thin translucent skin, and facial characteristics such as a pinched nose. Nov 19, 2019 · 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 monitoring. The game kicks off Dec. Does hypermobility worsen during pregnancy? Find out more about Hypermobile Ehlers-Danlos Syndrome using our easy to navigate body map. My cardiologist suspected and informed me about hEDS. This article compares the main signs and symptoms of vEDS and hEDS. 5-point favorites, and the total for this game is 50. How can we get a definite diagnosis one vs the other. hEDS is more than “just GJH” plus a few items from a checklist of findings. Red Sox predictions for June 30. But if you do have these symptoms it's better to be tested because the medical grade genetics test for vEDS is extremely accurate, and because vEDS is dangerous. Myopathic EDS (mEDS) Periodontal EDS (pEDS) Spondylodysplastic EDS (spEDS) Vascular EDS (vEDS) #TogetherWeDazzle Sign up to The Ehlers-Danlos Society mailing list Click here to sign up Hypermobile EDS (hEDS) Hypermobile EDS (hEDS) is the most common type, marked by joint hypermobility. The Types of EDS There are several forms of EDS. Washington Nationals MLB game, final score 5-0, from July 23, 2025 on ESPN. Hypermobile EDS (hEDS): The most common subtype, lacking an identified genetic cause and diagnosed clinically based on specific criteria for joint hypermobility and associated features. Philadelphia 10,000 times and revealed its MLB picks Visit ESPN for Cincinnati Reds live scores, video highlights, and latest news. Jul 4, 2025 · Phillies vs. My hands and feet are aged, my veins are prominent, and I have some vEDS facial Summary There are 13 different types of EDS, but they do have some clinical features in common. Additional Skin Findings in EDS Several unique dermatological findings are associated with EDS: Piezogenic Papules These small, soft, skin-colored lumps appear on the heels due to fat herniation under pressure. Is it more likely that I have vEDS? Thank you for any help on this. [3] Complications may include aortic dissection, joint dislocations, scoliosis, chronic pain, or early osteoarthritis. Facial Features of Marfan Syndrome Questions about vEDS vs hEDS I’ve already posted on here about my “old” looking hands (I’m 30 and my hands have looked like old lady hands since I can remember) and I have a few questions. Apr 3, 2023 · Patients with vEDS or LDS experienced significantly less depression, pain, fatigue and sleep problems compared with people with hEDS. Other common signs include easy bruising, atrophic scars, and poor wound healing. Learn about Vascular Ehlers-Danlos Syndrome (vEDS) and it's signs and symptoms. This is a community for people who have Vascular Ehlers Danlos Syndrome (or Ehlers Danlos Syndrome Type IV), are suspected of having vEDS, and their caretakers, friends and/or family. Dec 17, 2024 · Hypermobile EDS (hEDS) The most common subtype, known for joint hypermobility, chronic pain, and frequent joint dislocations. Ehlers–Danlos syndromes (EDS) are a group of 13 genetic connective tissue disorders. Please use other methods of research for that and talk to your doctor Jul 29, 2025 · CINCINNATI -- In some ways, the Dodgers had no business coming out on top of Tuesday night's 5-4 win over the Reds at Great American Ball Park. We follow patients with diagnoses of VEDS in our Connective Tissue Disorder Program here at Lurie Children’s. One of the most notable differences between “normal” and hEDS participants is the degree to which their skin is soft, stretchy, fragile, easily bruised, and has poor wound healing. HSD The most significant difference between hEDS and HSD lies in their diagnostic criteria. Morissette et al. Cincinnati Reds 10,000 times and Skin findings in vEDS include easy bruising and bleeding, atrophic scars, and acrogeria. Skin may be soft and slightly stretchy, but less than in other types. 2 days ago · Odds Shark previews the Big 12 Championship Game between BYU and Texas Tech. In contrast to other types of EDS that are characterized by hyperextensible, smooth, velvety skin, vEDS is characterized by thin and translucent skin with visible veins, but without hyperextensibility (39). It is linked to COL3A1 gene mutations. Local Interpretable Model-agnostic Explanations highlighted facial regions already established to characterize the facial features of vEDS 2 days ago · The Red Wings face off with a Bruins team that is much improved after a disappointing 2024-25 season. Jun 30, 2025 · The Cincinnati Reds and Boston Red Sox open a 3-game set Monday at Fenway Park. Navigate the body map to learn more about the condition. The main thing that should make you suspect vEDS is if you have family history of early death from a vascular event or have had a vascular event yourself. People with hEDS often experience chronic joint pain and instability. Mutations in this gene effect the production of type III collagen. “Patients Learn about Vascular Ehlers-Danlos Syndrome (VEDS), how it affects the body and who is affected from The VEDS Movement, a division of The Marfan Foundation. Learn More. This makes everyday activities challenging and painful. While EDS is known to be caused by mutations in genes affecting collagen and other connective tissue components, researchers are still working to fully understand its genetic underpinnings . For most types, such as hypermobile EDS (hEDS) and classical EDS (cEDS), life expectancy is generally normal, with patients facing chronic symptoms like pain, joint instability, and skin fragility rather than life-threatening complications. The Cincinnati Reds on Tuesday closed out spring training with an exhibition Jul 10, 2021 · No, almost all type of EDS has stretchy skin. Share your stories, struggles, successes, and any vEDS related information here! This is not the place to ask whether or not you have vEDS. Features, causes and diagnostic criteria Of the thirteen types, the four main types of EDS are: Hypermobile EDS (hEDS) Prevalence: Although official figures still state the prevalence of hypermobile Ehlers-Danlos syndrome in the population as being around 1 in 5000 people, it is generally acknowledged that the actual prevalence is far higher. Type III collagen is a protein which is found throughout the body including skin, blood vessels and hollow organs (such as Vascular Ehlers-Danlos Syndrome is a rare and severe form of Ehlers-Danlos Syndrome, affecting the connective tissues that provide structure and strength to the body's blood vessels and organs. May 17, 2024 · Understanding Vascular Ehlers-Danlos Syndrome (VEDS), a rare genetic disorder affecting collagen production in the body. Learn more! The hypermobile type (hEDS) is the most common, characterized by overly flexible joints that easily dislocate, stretchy skin, and various systemic issues. Boston finished at the bottom of the Atlantic, but has turned things around thanks to a Visible veins, especially if you are pale, is common in hEDS. Find standings and the full 2025 season schedule. 5 points. Whilst there are common features between many of the EDS types, there is less in common between hEDS and vEDS as can be seen in table 1, especially with regard to the vascular and hollow organ complications. Looking through the list of types might seem a little daunting, but for the majority of individuals the diagnosis is most likely to be the Hypermobile type (hEDS) (which we talk about separately, here), followed by the Classical (cEDS), then the Vascular type (vEDS). by Kia Reds Game Recap News Official Releases News Around Reds Country Vascular Ehlers-Danlos Syndrome (vEDS) is a rare and severe subtype of Ehlers-Danlos Syndrome (EDS), a group of inherited disorders affecting connective tissue. Reds odds, line, prediction, start time: 2025 MLB picks, July 4 bets from proven model SportsLine's model simulated Cincinnati vs. Learn about symptoms, diagnosis, and management at The Cardiovascular Care Group. Oct 18, 2024 · The AI classifier showed excellent performance with as few as 13 vEDS training images and distinguished vEDS from both controls and individuals with hEDS with high accuracy, achieving an area under the receiver operating characteristic curve ≥ 0. I feel like my diagnosis was basically a look over and that was it but when I read on vascular vs hypermobile, vascular was significantly scarier. Nov 18, 2025 · Preview the Nov. May 22, 2020 · Here are some of the differences between VEDS and the most common type of EDS, hEDS. Jan 1, 2025 · The AI classifier showed excellent performance with as few as 13 vEDS training images and distinguished vEDS from both controls and individuals with hEDS with high accuracy, achieving an area under the receiver operating characteristic curve ≥ 0. This is modest This feature, combined with fragile blood vessels, contributes to the unique presentation of vEDS. ofc i have to get the genetic testing (of which i did already, waiting results) as i do have a family history of ppl dying at a very young age due to vascular issues (which isn’t typical of c/hEDS and sounds more like vEDS but that aside…) This information is intended for people who have been recently diagnosed with vascular Ehlers-Danlos syndrome (vEDS) and their friends and relatives. 97.