Eds skin vs normal skin. Before participating, please read our rules.
Eds skin vs normal skin Authoritative facts from DermNet New Zealand. There are currently 14 proposed sub‐types, all of which display skin features within the minor and/or major criteria for diagnosis of Ehlers‐Danlos syndrome. Dermatologist Dr. Skin related symptoms: itching What are the craniofacial features of EDS? The craniofacial features of Ehlers-Danlos Syndrome vary significantly by subtype. Same with the skin on my arms. Normal for EDS skin, but this is NOT normal scarring for people without EDS. All types of EDS can cause changes in the skin, but not everyone with a type of EDS has skin features. A review of the literature suggests the five primary dermatological changes associated with hypermobile EDS are soft skin Jan 20, 2021 · How may EDS affect your skin? Although specific symptoms vary, most types of EDS have some degree of skin involvement. If you have hypermobile EDS, common signs include unusual joint flexibility and slightly stretchy skin. Patients are affected with joint hypermobility, skin hyperextensibilty, and skin fragility leading to atrophic scarring and significant Nov 11, 2016 · Bloom finally got an answer about 12 years ago at age 24, when she was diagnosed with Ehlers-Danlos Syndrome, a heritable cluster of disorders that can affect connective tissues like the skin and Nov 7, 2023 · Ehlеrs-Danlos syndromе (EDS) is a group of gеnеtic disordеrs that affеct connеctivе tissuеs, including thе skin. ” Fact: Hyper-elastic skin is an indicator for classic types of EDS, but is not typical for all types. Stretchiness, abnormal scarring, stretch marks at a young age, easy bruising and slow wound healing are all signs of EDS, but the presence and severity of these issues will depend on the type. This picture shows the unusually elastic skin (can be stretched much further than normal skin) of a patient with Ehlers-Danlos syndrome, a condition that affects connective tissues. This article explores various reasons skin might appear stretchy, including and beyond Ehlers-Danlos Syndromes. May 1, 2018 · Because Ehlers-Danlos syndrome (EDS) is still not as well-known as it should be, it often gets described in basic terms so others can more easily understand it: It’s a condition that causes dysfunction in the connective tissue, resulting in joint hypermobility, fragile tissue, and hyperflexible skin. Gastrointestinal tract symptoms: diarrhoea, nausea with vomiting and crampy abdominal pain. Hypermobile EDS is the least severe type of this disorder Hypermobile EDS is a genetic condition, but the cause of this condition isn’t clear. Seeking treatment for Ehlers-Danlos syndrome skin related issues? Learn about symptoms, causes, and treatment options at Advanced Dermatology. Some features, like translucent skin, may be harder to see on brown or black skin. People with EDS often have skin that can stretch well beyond normal limits. Explore treatments for stretchy skin in Ehlers-Danlos Syndrome and learn ways to enhance skin elasticity. But understand that skin hyperextensibility varies widely. Dray on 12 skin signs of hEDS. But some of it is also genetic regardless of EDS. This is modest When it comes to skin health, understanding the differences between normal skin and conditions like Ehlers-Danlos Syndrome (EDS) can be eye-opening. To systematically review the cutaneous features and adjunct investigations of EDS. May 12, 2015 · Basically it is looking for any spot on the body where “normal” people don’t have excess skin. Then my friends pinched me and screamed. People with EDS often have soft, velvety skin due to connective tissue abnormalities, which may give the appearance of youthful skin. May 19, 2022 · Myth: “You don’t have stretchy skin, so you can’t have EDS. While noticeably stretchy skin can indicate a medical condition, a degree of elasticity is normal and healthy. We would like to show you a description here but the site won’t allow us. I always thought skin should be stretchy, like at least an inch up. Lung related symptoms: wheezing, shortness of breath and harsh noise when breathing (stridor) that occurs with throat swelling. When it comes to skin health, understanding the differences between normal skin and skin affected by Ehlers-Danlos Syndrome (EDS) is crucial. Key Findings Abnormal Collagen Nanostructures: The study reveals that the collagen fibrils in the skin of EDS patients show significant deviations from normal nanostructures. This condition also causes skin to be easily bruised, heal poorly, form cigarette paper scars, and joints that are unusually flexible (hyperflexible, hypermobile). These were compared with normal values from 63 healthy children. Skin, Normal, Normale And More Mast Cell Activation Syndrome Heart related symptoms: rapid pulse (tachycardia), low blood pressure (hypotension) and passing out (syncope). Normal skin typically exhibits elasticity and resilience, while EDS presents unique challenges due to its hyper-elasticity and fragility. Anyone else have stretchy skin as well? Note a geneticist says I do NOT have EDS or any other tissue disorder before anyone says anything. This is a welcoming place for those affected (or those simply wanting to learn more) to ask questions, share successes and failures, feel less alone, and discuss everyday life. Jul 15, 2022 · The Ehlers-Danlos syndromes (EDS) are a group of inherited connective tissue disorders with variable cutaneous fragility, joint hypermobility and systemic manifestations. Stretch marks, or striae, are a common skin condition characterized by streaks or lines that develop when the skin is stretched rapidly. I’ve seen firsthand how EDS can manifest in various ways, making it essential to recognize the unique characteristics of this condition. Oct 14, 2021 · People who suffer from Ehlers-Danlos syndrome (EDS) may experience bladder issues such as stress incontinence or infection in the bladder. The skin on my hand can be stretch around 2 inches up. Skin naturally stretches and recoils. EDS is a painful condition that causes joint hypermobility, dislocations, dysautonomia, poor wound healing, stretchy or velvety skin, and so many debilitating symptoms. Skin hyperelasticity is a clinical hallmark of hypermobile Ehlers–Danlos syndrome and falls under Criterion 2 Feature Abstract Objective: The criteria for Ehlers-Danlos syndrome (EDS) and the hypermobility syndrome (HMS) should be reliable. Gentle hugs Cutaneous manifestations are a diagnostic criterion of Ehlers-Danlos syndrome, hypermobility type (EDS-HT) and joint hypermobility syndrome (JHS). An overview of skin related signs and symptoms in common hypermobility related conditions. New comments cannot be posted and votes cannot be cast. A review of the literature suggests the five primary dermatological changes associated with hypermobile EDS are soft skin, atrophic Download scientific diagram | (A,B): Skin and joint hyperelasticity from publication: Classical Ehlers-Danlos syndrome: Clinical, Histological and ultrastructural aspects | A 12-year-old boy with Sep 13, 2019 · People with Ehlers-Danlos syndrome have skin that is fragile and easily broken, which makes skin care challenging, so here are five tips that may help. However, their skin is also fragile and prone to premature aging under environmental stressors like UV exposure. 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. This hyperextensibility is often accompanied by softness and a velvety texture, especially in the early stages of the disorder. Stretchy skin can occur in almost all subtypes of EDS, being most prominent in classical EDS. Before participating, please read our rules. Noninvasive measurements were performed under suction of 500 mbar using a Cutometer equipped with a 4 … Download scientific diagram | shows this patient’s skin hyper elasticity. Hypermobility, where various joints of the body move beyond what is considered to be normal, is a more common trait for all forms of EDS. Problems with connective tissue can cause changes in the skin. Do you consider my skin stretchy or my joints to be hypermobile? By no means I ask you to diagnose me. Cutaneous and orthopedic features in five members of the EDS family. The cutaneous (skin) hallmarks of the Ehlers-Danlos syndromes (EDS) are variable depending on the subtype. The Ehlers-Danlos syndrome (EDS) is a clinically and genetically heterogeneous connective tissue disorder affecting as many as 1 in 5,000 individuals (1). Tissue fragility in EDS can also lead to hernias and problems in pregnancy. A search of PubMed and Web of Science for EDS-related cutaneous features and additional investigations was undertaken from publication of the 2017 International Classification of EDS until January 15, 2022. I’ve been meaning to go through tests for eds because joint and muscle pain and bad wound healing but I don’t want to embarrass myself during appointment by having stuff that’s considered normal. EDS is genetic, so if someone in your family has it, you may too. Fragile skin is also a common manifestation of EDS, especially in people with the classic, kyphoscoliotic, and periodontitis types. It has to do with the nature of how it stretches and not just the distance from base level. Classical and dermatosparaxis EDS are examples of types with a lot of skin involvement, but Jul 10, 2021 · No, almost all type of EDS has stretchy skin. My neck is by far the stretchiest, if i’m not wrong around 4 inches. So it’s not that normal people can’t have skin that’s considered “very soft” like ours, but for people who don’t have EDS it usually requires effort and/or beauty products? If that makes sense. Nov 20, 2024 · In explaining how Ehlers-Danlos syndrome affects connective tissue, I am also comparing and contrasting the function and structural characteristics of tissues. The Ehlers‐Danlos syndromes (EDS) are a group of inherited connective tissue disorders with variable cutaneous fragility, joint hypermobility and systemic manifestations. P2: eyelid skin redundancy and skin hyperextensibility over the neck (a); skin wrinkling over knees, tights (b), and abdomen (c Classic EDS: skin is a significant finding Vascular EDS: arterial ruptures/dissections Many other forms, but most are extremely rare and have severe phenotypes from a young age. The different structure of the skin in the Ehlers-Danlos syndromes makes it more fragile than normal skin. : r/Hypermobility Gaming Sports Business Crypto Television Celebrity r/Hypermobility r/Hypermobility This picture shows the unusually elastic skin (can be stretched much further than normal skin) of a patient with Ehlers-Danlos syndrome, a condition that affects connective tissues. My mom is diagnosed, and my sister saw a geneticist but didn’t meet the criteria. EDS is characterized in its most common form by hyperextensibility of the skin, hypermobility of joints often resulting in dislocations, and tissue fragility exemplified by easy bruising, atrophic scars following superficial injury, and Nov 2, 2023 · Ehlers-Danlos Syndrome (EDS) is a hereditary condition that affects the skin and the mobility of joints due to abnormal collagen synthesis. Mar 29, 2023 · Vascular Ehlers–Danlos syndrome (vEDS) is a particular type of EDS characterized by multiple organ fragility, arterial, intestinal, and/or uterine; patient’s skin appears thin and translucent; among the general clinical aspects of the disease, are included easy bruising, characteristic facial appearance (thin vermilion of the lips Sep 1, 2024 · Ehlers-Danlos Syndrome (EDS) is a genetic disorder affecting connective tissue, causing joint hypermobility & skin elasticity. Jun 1, 2021 · Ehlers–Danlos syndrome (EDS) is a group of inherited connective tissue disorders that may present with a wide range of multisystemic symptoms. But, in hEDS (Hypermobile Ehlers Danlos Syndrome), you have only a minimal amount of elastic skin. Abstract Ehlers–Danlos syndrome (EDS) is a group of inherited connective tissue disorders that may present with a wide range of multisystemic symptoms. Ehlers-Danlos syndrome (EDS) is a group of conditions that are genetically inherited. There are currently 14 proposed sub-types, all of which display skin features within the minor and/or major criteria for diagnosis of Ehlers-Danlos syndrome. Vascular EDS (vEDS) is a rare type of EDS. Vascular EDS is often associated with large, prominent eyes, a small chin, sunken cheeks, thin lips, and translucent skin that can reveal veins. Mar 21, 2025 · Diagnosing Ehlers-Danlos Syndrome Common symptoms of Ehlers-Danlos Syndrome (EDS) include overly flexible joints and stretchy, fragile skin. Connective tissue is found throughout the body and is an important component of the skin. • What is Ehlers-Danlos Syndrome? The Ehlers-Danlos syndromes (EDS) are a group of heritable connective tissue disorders. It is inherited in an autosomal dominant way which means that if a person has vEDS there is a 50% […] Classical EDS is a heritable disorder of connective tissue. But when I reach my eyelids I could probably do 3 inches but it’s hard to measure there. Over time, the skin may become thin, translucent, or wrinkled, making underlying blood vessels more visible and Watch short videos about eds skin vs normal skin from people around the world. These two conditions, originally considered We would like to show you a description here but the site won’t allow us. Ehlers Danlos Syndrome and Stretch Marks Guide Ehlers Danlos Syndrome is a group of inherited disorders that affect the body’s connective tissues, primarily involving the production of collagen. Definitely an atrophic scar, sometimes referred to as cigarette paper scars. What is the pinch test for Ehlers-Danlos syndrome skin? The pinch test involves gently pinching the skin to assess its elasticity and ability to return to normal shape. The skin changes in hypermobile EDS (hEDS) tend to be less pronounced than in classical EDS (cEDS) although they can overlap with the milder forms of cEDS. Hypermobile EDS, one of 13 identified subtypes of EDS, is the only variant without a known associated genetic mutation. Sep 25, 2025 · Ehlers-Danlos syndrome (EDS) is a connective tissue disorder that causes joint hypermobility, skin hyperextensibility, and tissue fragility. There are 13 different types of EDS, but they do have some clinical features in common. Jul 16, 2025 · Fragile skin is also a common manifestation of EDS, especially in people with the classic, kyphoscoliotic, and periodontitis types. Talk to your doctor or a genetic disease specialist about your symptoms: they may be able to diagnose you using genetic testing. Pеoplе with EDS havе skin that is morе fragilе, strеtchy, and bruisе-pronе than normal skin. One of the hallmark skin signs of Ehlers-Danlos Syndrome is hyperextensibility. How do I find an image or chart of varying degrees of hyper elasticity in skin? A ‘normal’ pinch test vs and EDS affected pinch test? Archived post. One of the most common traits is overly stretchy skin (hyperextensible), which can stretch farther than normal. . The reason for this is because EDS is the result of defects in the type of collagen your body Jan 20, 2025 · It is important to point out that there are normal age-related changes in collagen that happen to everyone, which lead to more body-wide changes like skin aging, osteoporosis, and osteoarthritis (1). So skin seems normal in the early stages of hEDS. As someone who’s intrigued by dermatological variations, I find it fascinating how these differences impact An EDS specialist pinched the skin on my hand (which doesn’t stretch far at all) and say yep that’s EDS stretchy skin. This is a support sub for those with Ehlers-Danlos syndrome (all types) and HSD—diagnosed or waiting to be diagnosed. Unlike the well-organized and tightly packed collagen fibrils seen in healthy individuals, those in EDS patients tend to be disorganized and irregular in shape and size. Mechanical properties of skin were evaluated in vivo in 17 children suffering from Ehlers-Danlos syndrome (EDS) types I, II, and III. So it is one possible manifestation of EDS that can be used in diagnosing which type of EDS, but it certainly would not rule out a diagnosis. Discover the key skin signs in EDS and HSD including how to identify skin softness, hyperextensibility, unique scars, and other important features. Hypermobile EDS diagnosis is easy to miss, but these signs and symptoms can be a clue Sep 11, 2025 · Ehlers-Danlos syndrome is a group of genetic disorders that affect the connective tissues and cause symptoms such as stretchy skin and loose joints. Hypermobile Ehlers-Danlos Syndrome Skin Signs Not To Miss. Examination for general joint hypermobility has high reliability but there is only sparse information on the reliability of skin tests, and no information on the level of normal skin extensibility. While stretch marks can occur for various reasons, individuals Mar 13, 2018 · EDS can be divided into 13 different subtypes, each involving different signs and symptoms, but is commonly characterized by joint hypermobility (joints that stretch further than normal), skin hyperextensibility (skin that can be stretched further than normal), and tissue fragility. Ehlers–Danlos syndrome, EDS, Cutis hyperelastica dermatorrhexis, Dystrophia mesodermalis congenita, India rubber skin, Hereditary collagen dysplasia, Cutis elastica, Cutis hyperelastica, Danios disease, Fibrodysplasia elastica generalisata, Meekeren-Ehlers-Danlos syndrome, Dermatorrhexis with dermatochalasis and arthrochalasis. These can include joint hypermobility, stretchy skin and tissue fragility.