Eds syndrome They can range from mild to life-threatening. This article will explore the relationship between EDS and scoliosis, what it means for those affected, and the treatment options Ehlers-Danlos Syndrome (EDS) presents a unique set of challenges in the field of anesthesia. People with EDS may have fragile skin or unstable joints. Arousals and awakenings during the night can interfere with the sleep cycle and prevent a person from getting Ehlers-Danlos Syndrome (EDS) is controversial because it’s misunderstood, underdiagnosed, and stigmatized. There are several different types Brittle Cornea Syndrome (BCS) Cardiac-valvular EDS (cvEDS) Classical EDS (cEDS) Classical-like EDS (clEDS) Dermatosparaxis EDS (dEDS) Hypermobile EDS (hEDS) Hypermobility Spectrum Disorders (HSD) You could win an amazing prize pack, courtesy of Rebecca Yarros! Rebecca is a #1 New York Times Bestselling Author, and her Fourth Wing fantasy book series follows the story of Violet Sorrengail, who has Ehlers-Danlos syndrome (EDS), a diagnosis Rebecca shares. Ehlers-Danlos syndrome can affect the skin, joints, and blood vessels. The genetic cause (s) of hEDS have not been identified. Symptoms often include loose joints, joint pain, stretchy, velvety skin, and abnormal scar formation. Ehlers-Danlos syndromes (EDS) are a diverse family of heritable connective tissue disorders traditionally characterized by hypermobile joints, stretchy skin, and tissue fragility. Many individuals with EDS, especially those with hypermobile Ehlers-Danlos Syndrome (hEDS), experience a range of GI disorders that can significantly impair Apr 22, 2024 · If you have vascular Ehlers-Danlos or EDS with severe symptoms that prevent you from working, you may be able to get Social Security disability benefits. Symptoms include: Loose joints Fragile, small blood vessels Abnormal scar formation and wound healing Soft, velvety, stretchy skin that bruises If you or a loved one suffers from Ehlers-Danlos Syndrome (EDS), you need to find a comprehensive treatment center that will empower you and improve your well-being. In this article, we will take a closer look at wide range of famous people with hypermobility as well as those with hypermobility due to Ehlers Danlos Nov 12, 2021 · Many patients with hypermobility spectrum disorder (HSD) and hypermobile EDS (hEDS) either have symptoms of or have been diagnosed with “POTS” or “dysautonomia”. Ehlers-Danlos syndromes (EDS) are a group of inherited connective tissue disorders caused by abnormalities in the structure, production, and/or processing of collagen. Symptoms of EDS can include joint pain or popping, joint dislocation or instability, flat feet, back pain, and easily bruised or stretchy skin. Figures may be presented in different ways, but they mean the Ehlers-Danlos syndrome (EDS) is a disorder that affects the body's connective tissues. Understanding their connection is vital for effective diagnosis, treatment, and management. The symptoms of EDS vary by type and range from mildly loose joints to serious complications. Click the button to find What is Ehlers-Danlos syndrome? Ehlers-Danlos syndrome (EDS) is a group of rare genetic disorders. Voermans, adapted by Benjamin Guscott The Ehlers–Danlos syndromes (EDS) are a mixed group of connective tissue disorders characterized by overly moveable joints, stretchy skin, and Aug 10, 2022 · Ehlers-Danlos syndrome is a group of inherited connective tissue disorders that primarily affects the skin, joints, and blood vessel walls 1 but can affect every organ system and result in significant morbidity and mortality. Understanding EDS and Its Types EDS encompasses 13 different Hypermobile Ehlers-Danlos Syndrome (hEDS) and Hypermobility Spectrum Disorders (HSD) are connective tissue disorders characterized by joint hypermobility, chronic pain, and a range of systemic symptoms. About 1 in 5,000 people has EDS. Collagen, a vital component of connective tissue, plays a key role in providing strength and elasticity to the skin, joints, blood vessels, and internal organs. Orthopedics is the medical specialty that deals with those problems. Sep 7, 2025 · Ehlers-Danlos syndrome is a group of genetic connective tissue disorders classified in 13 types. We hope the following is a helpful summary. Managing pregnancy in individuals with EDS requires careful What is EDS? Ehlers-Danlos Syndrome (EDS) is a condition characterized by fragile skin and overly flexible joints. These tissues provide support to the skin, bones, blood vessels, and other organs. It can be inherited from a parent with the same faulty gene, alternatively someone can be born with a new mutation so that the condition is What is Ehlers-Danlos syndrome? Ehlers-Danlos syndrome (EDS) is a group of inherited disorders involving connective tissue in the body. This article Apr 10, 2022 · Vascular Ehlers-Danlos Syndrome Vascular-type Ehlers-Danlos syndrome is a severe subtype of a genetic connective tissue disorder. He and his team at the Center provide care for the numerous complications of EDS: joint pain, headaches, POTS, GI problems, and mast cell activation syndrome. At this center, you’ll learn about treatment options for EDS, and discover how EDS patients can improve their quality of life. Ehlers-Danlos Syndrome is a constellation of many different disorders, all sharing to some degree a defect in a patient’s connective tissue that makes that tissue fragile and stretchy. , Claudiu Austin, Edward Benzel, Paolo Bolognese, Richard Ellenbogen, Clair A. There is no up-to-date research to tell us exactly how frequently it occurs. EDS may manifest simply as extra-flexibility in one Oct 31, 2024 · Living with Ehlers-Danlos syndrome (EDS), especially the hypermobile type (hEDS), can present a host of symptoms that often go undiagnosed in childhood. Connective tissue is a supporting structure in our body and is made up of a number of proteins including collagen, which is the protein most often thought to be […] Ehlers-Danlos Syndrome (EDS) is a complex condition that affects many parts of the body. The Ehlers-Danlos syndromes are a group of heritable connective tissue disorders. Here are 23 signs that might reveal a childhood spent adapting to life with EDS. Ehlers–Danlos syndromes (EDS) are a group of 13 genetic connective tissue disorders. EDS usually affects your skin, joints and blood vessel walls. While the genetic Ehlers-Danlos syndrome (EDS) is a group of genetic disorders that affect the connective tissues of the body. There are several types of EDS. Saperstein has diagnosed and treated over 500 patients with EDS. Given the complexities of connective tissue disorders, it Ehlers-Danlos syndrome (EDS) is a group of connective tissue disorders that can occur in families. [1] . It is estimated that up to 70% of HSD/hEDS patients report symptoms consistent with dysautonomia and up to 40% meet diagnostic criteria for POTS. Brandon Colby MD Introduction Ehlers-Danlos Syndrome (EDS) is a group of rare genetic disorders that affect the connective tissues in the body. Defects in connective tissues cause the signs and symptoms of these conditions, which range from mildly loose joints to life-threatening complications. Map results may not be 100% accurate. Ehlers-Danlos syndrome (EDS) is a group of rare genetic disorders. What makes a condition “rare”? A condition is considered rare if it affects less than 1 in 2000 people. People with EDS or HSD may also wake up during the night due to pain, joint instability, and other symptoms. Unlike other forms of EDS, hEDS currently has no known genetic marker, and diagnosis is based on clinical criteria, including family history, hypermobility scoring, and the presence of Fraser C. What is Ehlers-Danlos syndrome? Ehlers-Danlos syndrome (EDS) is a group of rare genetic disorders. Navigate the body map to learn more about the condition. Ehlers Danlos syndrome (EDS) is a group of hereditary connective tissue disorder s which manifests clinically with skin hyper-elasticity, hypermobility of joints, atrophic scarring, and fragility of blood vessels. Fluoroquinolones are a class of antibiotics commonly prescribed to treat various bacterial infections. Collagen is a type of protein. Feb 21, 2017 · – characterized by joint hypermobility, skin extensibility, and tissue fragility. Testing schedules may vary. Find out what causes this condition and how it's treated. If EDS is suspected, an early confirmed diagnosis is imperative to keep the condition from getting worse. This may result in complications ranging from increased bruising, loose joints, chronic pain, and some Understanding Ehlers-Danlos Syndrome (EDS) Author: Dr. Extraordinary Flexibility: You might have amazed others with your ability to perform “party tricks” with hypermobile joints, like bending your fingers Ehlers-Danlos Syndrome (EDS) is a complex disorder and shares overlapping symptoms with other connective-tissue disorders, as well as other common conditions. EDS is an underdiagnosed genetic condition The prevalence of the Ehlers-Danlos syndromes (EDS) and hypermobility spectrum disorders (HSD) Our community may read different commentaries about prevalence figures for EDS and HSD. This communication briefly reports upon the neurological manifestations that arise including the weakness of the ligaments of the craniocervical junction and spine, early disc degeneration, and the weakness of the epineurium and perineurium surrounding peripheral nerves. In . One of the more complex and challenging conditions that frequently coexists with EDS is dysautonomia, a disorder that affects the autonomic nervous Sep 23, 2024 · INTRODUCTION The Ehlers-Danlos syndromes (EDS) are a group of conditions that are characterized by one or more of several common features: skin hyperextensibility, joint hypermobility, and tissue fragility. People who have Ehlers-Danlos syndrome usually have overly flexible joints and stretchy Ehlers-Danlos Syndrome (EDS) is a group of genetic connective tissue disorders that affects the body in many ways, including the spine. Get expert advice from UT Southwestern Medical Center men's and women's health specialists. Learn about the symptoms, causes, and diagnosis of each type of EDS, and how they are inherited. Part 1 of this series focused on challenges and developments in the diagnosis of Ehlers-Danlos syndrome (EDS). Among the subtypes, hypermobile Ehlers-Danlos Ehlers-Danlos syndrome (EDS) id a rare genetic disorder affecting connective tissue. Entrapment, deformation, and biophysical Sep 23, 2024 · Comprehensive guide on clinical manifestations and diagnosis of Ehlers-Danlos syndromes, including symptoms, diagnostic criteria, and management strategies. While effective in combating infections, they are also associated with severe side effects, particularly for individuals with connective tissue disorders such as Ehlers-Danlos Syndrome (EDS), Marfan Syndrome, and Loeys-Dietz Syndrome. Connective tissues are proteins that support skin, bones, blood vessels, and other organs. Ehlers-Danlos Syndrome (EDS) is a group of genetic disorders of the connective tissue. Sep 11, 2025 · Ehlers-Danlos syndrome (EDS) is a group of genetic disorders that affect the body’s connective tissues, including those in the joints, skin, and blood vessels. Given its complexity and the wide spectrum of symptoms and associated conditions, finding specialized care is often difficult for individuals living with EDS. People with EDS typically have loose joints and stretchy skin. A more severe form of the disorder Hypermobile Ehlers-Danlos syndrome (hEDS), which used to be known as the hypermobility type or type 3, is thought to be the most common genetic connective tissue disorder. Therefore, a patient will want to seek out Abstract Ehlers-Danlos syndrome (EDS, ORPHA98249) comprises a group of clinically and genetically heterogeneous heritable connective tissue disorders, chiefly characterized by joint hypermobility and instability, skin texture anomalies, and vascular and soft tissue fragility. In addition, there are 13 types of EDS alone – with varying treatments. What is EDS? The Ehlers-Danlos syndromes (EDS) is the name given to a group of non-inflammatory hereditary conditions, which are all disorders of the connective tissue. Learn about Vascular Ehlers-Danlos Syndrome (vEDS) and it's signs and symptoms. Aug 25, 2022 · People who have Ehlers-Danlos syndrome usually have overly flexible joints and stretchy, fragile skin. Children who have EDS typically have overly flexible joints. As a progressive collaboration Learn about hypermobility spectrum disorder (HSD), diagnosis, management, causes and how it affects the different parts/systems of the body. Most babies Ehlers-Danlos Syndrome (EDS) is a group of inherited connective tissue disorders characterized by joint hypermobility, skin hyperextensibility, and tissue fragility. What Are EDS and POTS? Ehlers Complex Regional Pain Syndrome (CRPS) and Ehlers-Danlos Syndrome (EDS) Complex Regional Pain Syndrome (CRPS) and Ehlers-Danlos Syndrome (EDS) are two distinct conditions that share significant overlaps in their pathophysiology, clinical manifestations, and challenges in diagnosis and treatment. As awareness of EDS grows, researchers and clinicians Ehlers-Danlos Syndrome (EDS) is a rarely diagnosed but surprisingly common genetic disorder that affects connective tissues in the body. Ehlers-Danlos syndrome (EDS) is a genetic condition that weakens your connective tissue. While it may not be on everyone's radar, there are actually quite a lot of celebrities who live with EDS. Henderson Sr. Ehlers-Danlos syndrome is a group of disorders that affect connective tissues supporting the skin, bones, blood vessels, and many other organs and tissues. However, a lesser-known aspect of EDS is its impact on the gastrointestinal (GI) system. These conditions often involve joint hypermobility, chronic pain, fatigue, and other multisystem issues that can affect quality of life. Our EDS program is available at the NYIT Academic Health Centers. The conditions are distinguished by family history and clinical criteria, including the degree and nature of involvement of skin, joints, skeleton, and vasculature [1]. A recent international Ehlers-Danlos Syndrome (EDS) and Postural Orthostatic Tachycardia Syndrome (POTS) Ehlers-Danlos Syndrome (EDS) and Postural Orthostatic Tachycardia Syndrome (POTS) often coexist, presenting a complex clinical picture that significantly impacts patients' quality of life. Read about symptoms, diagnosis, management, genetic factors and more. Most children with EDS have hypermobile joints that are prone to full or partial dislocation. Each type is caused by pathogenic genetic variants that prevent connective tissue from functioning properly. It is largely diagnosed clinically, although identification of the gene encoding the collagen or proteins interacting with it is necessary to identify the type of EDS. EDS is a group of hereditary connective tissue disorders characterized by joint hypermobility, skin fragility, and vascular complications. Dystonia can manifest as repetitive twisting, tremors, or abnormal postures that result from these uncontrolled muscle movements. Sometimes, this leads to symptoms of postural orthostatic tachycardia Hypermobile Ehlers-Danlos Syndrome (hEDS) What is hypermobile Ehlers-Danlos syndrome (hEDS)? What is the prevalence of hEDS? What causes hEDS? H ypermobility s pectrum d isorders (HSD) are connective tissue disorders that cause joint hypermobility, instability, injury, and pain. The problems seen in EDS and HSD often go unconnected for many years. Facial Features of Ehlers-Danlos Syndromes Ehlers-Danlos Syndrome (EDS) is widely recognized for its effect on the connective tissues, leading to joint hypermobility, skin elasticity, and often, chronic pain. In Ehlers-Danlos syndrome (EDS) is a rare, genetically variable, heterogenous group of (currently recognized) thirteen connective tissue disorders characterized by skin hyperextensibility, tissue fragility, and generalized joint hypermobility. People with this condition have very fragile tissues and are at high risk for severe bleeding and internal injuries. Introduction Ehlers-Danlos Syndrome (EDS) is a group of heritable connective tissue disorders characterized by joint hypermobility, skin hyperextensibility, and tissue fragility. Although there are some overlaps, each condition has distinct facial presentations that assist in differential diagnosis. Signs and symptoms, and their severity, vary widely even for those in the same family. Nov 17, 2025 · Credit: Getty Images In part 2 of this series on Ehlers-Danlos syndrome (EDS), we spoke with Brittany Goss, DO, for an in-depth look at treatment considerations among patients with EDS. Efforts on recognition, diagnosis, and management of the presumed, most common connective tissue disorder hypermobile Ehlers-Danlos syndrome have been an ongoing challenge, even decades after the description of this condition. There are 13 recognized types of EDS, each with its unique genetic basis and associated symptoms. While musculoskeletal symptoms often dominate clinical attention, gastrointestinal (GI) issues are among the most common—and most under-recognized—manifestations of EDS Ehlers-Danlos syndrome (EDS) is a group of genetic disorders that affect the connective tissues. One of the complications that often arises in people with EDS is scoliosis, a condition that causes the spine to curve abnormally. Problems with collagen can affect many parts of the body, including the skin, joints, blood vessels, bones, cartilage, and tendons GI Issues in EDS: A Comprehensive Guide I. Ehlers-Danlos Syndrome (EDS) is an umbrella term for a heterogeneous group of inherited connective tissue disorders characterized by symptoms including, but not limited to, skin hyperextensibility, joint hypermobility, and vascular fragility. (However, there are several causes of hypermobility, and many children with Aug 12, 2024 · Ehlers-Danlos syndrome (EDS) is a connective tissue disorder. Singman, and Nicol C. Quality medical care and support for Ehlers Danlos Syndrome, Mast Cell Activations Syndrome, POTS, and related conditions Feb 17, 2021 · If you have Ehlers-Danlos syndrome (EDS) you may experience a variety of issues related to muscles, bones and joints. Other problems such as fatigue, headaches, GI problems, and autonomic dysfunction are often seen as part of HSD. Apr 9, 2024 · EDS is a genetic disorder that weakens your connective tissues, causing joint hypermobility, skin fragility, and organ issues. [7] . It adds strength and structure to organs and connective tissues. Orthopedic issues are among the most debilitating complications for individuals with EDS, largely due to the instability of joints, ligament laxity, and overall The term “Ehlers-Danlos syndrome” (EDS) groups together an increasing number of heritable connective tissue disorders mainly featuring joint hypermobility and related complications, dermal dysplasia with abnormal skin texture and repair, and Ehlers-Danlos Syndrome (EDS) refers to a group of disorders that affect the body’s connective tissue, including skin, tendons, ligaments and blood vessel walls. It can vary greatly in severity, and can affect the skin, blood vessels and joints. It is Learn about Ehlers-Danlos syndromes—a group of genetic connective tissue disorders. It can affect your skin, joints, muscles, blood vessels, organs and bones. How is it diagnosed? The diagnosis is usually first suspected through clinical Ehlers-Danlos Syndrome (EDS) is a group of hereditary disorders affecting connective tissues, characterized by joint hypermobility and a range of other symtpoms. Discover symptoms, types, diagnosis tips, and how to manage life with EDS. Introduction Ehlers-Danlos Syndrome (EDS) is a group of hereditary connective tissue disorders characterized by joint hypermobility, skin hyperextensibility, and tissue fragility. Connect, share experiences, and find understanding through the community. But beneath this surface-level definition lies a far more intricate story—one that's beginning to unfold thanks to emerging research on inflammation and biomarkers. Dr. These connective tissues provide strength and elasticity to other parts of the body. Learn about the symptoms, diagnosis, and treatment. The purpose of this post is to provide a brief overview of the answers to the 20 Orthopedic Issues in Ehlers-Danlos Syndrome: From Head to Toe Ehlers-Danlos Syndrome (EDS) is a group of connective tissue disorders that primarily affect the skin, joints, and blood vessel walls due to faulty collagen production. A quote from The Ehlers-Danlos Society’s website states: “We believe that hEDS and HSD are two of the most misunderstood conditions of our time, and we look forward to a time when robust research with clean phenotyped data can show that both hEDS and HSD are common, as we believe Ehlers-Danlos Syndrome (EDS) at a Glance The Ehlers Danlos Syndromes (EDS) is a group of hereditary connective tissue disorders that primarily affect the skin and joints. Managing Ehlers-Danlos syndrome Physical and Mar 31, 2023 · Ehlers-Danlos syndrome (EDS) is the name given to a group of more than 10 different inherited disorders; all involve a genetic defect in collagen and connective-tissue synthesis and structure. Ehlers-Danlos syndrome (EDS) is a group of inherited disorders marked by extremely loose joints, very stretchy (hyperelastic) skin that bruises easily, and easily damaged blood vessels. Twelve types of EDS have known genetic causes, and some types are associated with multiple different genes. Supportive devices such as braces, splints, and mobility aids provide vital assistance, enabling individuals to carry out daily activities while helping prevent injury. While it isn’t curable, this condition is often manageable, and the complications are often treatable. They sometimes also have fragile, stretchy skin. Rebecca recently collaborated with the Colorado Avalanche ice hockey team with a special edition jersey. 1 It is a result of genetic mutations that cause defects in the formation of types I, III, and/or V collagen, which can manifest with pathologies in Join Ehlers-Danlos Syndrome Support, a caring online community for patients and families living with EDS. Connective tissue is a complex mixture of proteins and other substances that provide strength and elasticity to the underlying structures in your body. Of its subtypes, hypermobile EDS (hEDS) is both the most common and complex to diagnose, presenting a wide array of physical and psychological challenges. Diagnosing EDS can be challenging due to its varied symptoms and overlapping characteristics with other conditions. Ehlers-Danlos syndrome (EDS) is a group of inherited disorders that weaken connective tissues. Nov 6, 2024 · Ehlers-Danlos syndrome (EDS) is a group of inherited disorders marked by extremely loose joints, very stretchy (hyperelastic) skin that bruises easily, and easily damaged blood vessels. Here's a guide on how EDS is tested and diagnosed. Explore symptoms, inheritance, genetics of this condition. Connective tissue is a complex mixture of proteins and other substances that provide strength and elasticity to the skin, bones, blood vessels, and other organs. 2 Typical clinical manifestations are skin hyperelasticity, hypermobility May 27, 2024 · Ehlers-Danlos Syndrome (EDS) physical therapy works by strengthening the muscles around the joints to improve stability, enhancing proprioception to prevent injuries, and managing pain through tailored exercises and modalities. Pain and other symptoms may make it difficult to get comfortable enough to fall asleep. This article explores their intersection, discussing underlying mechanisms, shared comorbidities Ehlers-Danlos Syndrome (EDS) is widely known for its effects on connective tissues, leading to joint hypermobility, skin elasticity, and chronic pain. What is hypermobility? Joint hypermobility means that a person’s joints have a greater range of motion than is expected or normal. Hypermobile Ehlers-Danlos Syndrome is the most common form of Ehlers-Danlos Syndrome, primarily characterized by generalized joint hypermobility, chronic pain, and frequent joint dislocations or subluxations. Problems with collagen can affect many parts of the body, including the skin, joints, blood vessels, bones, cartilage, and tendons Dec 18, 2023 · Ehlers-Danlos syndrome (EDS) affects the body's connective tissues. Individuals with hEDS and HSD often face additional complications like fatigue, gastrointestinal dysfunction, and nutritional deficiencies, primarily due to malabsorption and increased Turnaround time is defined as the usual number of days from the date of pickup of a specimen for testing to when the result is released to the ordering provider. In some cases, additional time should be allowed for additional confirmatory or additional reflex tests. These tools can be tailored to each person's unique needs and are most effective when used alongside a regular Mar 6, 2025 · Learn about diagnosing and treating Ehlers-Danlos syndrome, an 'invisible' disease. Like most illnesses, there isno cure for EDS or HSD, but there is a lot that can be done to reduce the symptoms Many people and healthcare professionals are still unfamiliar with the Ehlers-Danlos syndromes (EDS), the hypermobility spectrum disorders (HSD), and the complex ways in which these conditions can affect people’s lives. Genetic tests on a sample of your blood can confirm the diagnosis in rarer forms of Ehlers-Danlos syndrome and help rule out other problems. Sep 1, 2024 · Ehlers-Danlos Syndrome (EDS) is a genetic disorder affecting connective tissue, causing joint hypermobility & skin elasticity. Description Ehlers-Danlos syndrome is a group of disorders that affect connective tissues supporting the skin, bones, blood vessels, and many other organs and tissues. Comparison of Facial Features in Ehlers-Danlos Syndromes (EDS) and Marfan Syndrome Facial features play an important role in clinical recognition of Ehlers-Danlos Syndromes (EDS), particularly vascular EDS, and Marfan Syndrome. For hypermobile Ehlers-Danlos syndrome, the most common form, there is no genetic testing available. Find out more about Hypermobile Ehlers-Danlos Syndrome using our easy to navigate body map. Learn about the 13 types of EDS, how they're diagnosed, and how they're treated. Connective tissue provides support to many parts of body like skin, muscles, and ligaments. Find out how hEDS is diagnosed and can be managed. This can become a problem if you have a wound that requires stitches, because the skin often isn't strong enough to hold them. On the other hand, people with EDS have to be very careful about which exercises they participate in to avoid injury, and they often experience pain during the workout. This article addresses a few important questions often asked by those Aug 24, 2022 · Ehlers-Danlos syndrome is a group of inherited disorders that affect your connective tissues — primarily your skin, joints and blood vessel walls. Ehlers-Danlos Syndrome (EDS) is a group of inherited connective tissue disorders that impact the body’s collagen structure and function. It can affect blood vessel function and blood flow regulation. Each of these features can complicate anesthesia procedures, making it essential for anesthesiologists to fully understand the risks and tailor their approaches Jul 24, 2023 · Exercising with Ehlers-Danlos syndrome (EDS) is complicated. Living with Ehlers-Danlos Syndrome (EDS) often involves managing joint instability, pain, and frequent dislocations. While dystonia is common in the general population, its prevalence in EDS, particularly in the Whether you have Ehlers-Danlos Syndromes (EDS) or one of the Hypermobility Spectrum Disorders (HSD), many of the daily challenges are the same. However, for many individuals, the impact goes beyond these physical symptoms. Learn about diagnosis, symptoms and treatment from Froedtert & MCW specialists. These may be noticed at birth or in early childhood. Because of extensive research and better understanding of the disease, EDS is being identified more frequently, and it is estimated that one in 5,000-10,000 people in the world have this condition. Among the 13 recognized subtypes, Classical EDS (cEDS), Hypermobile EDS (hEDS), and Vascular EDS (vEDS) are the most commonly encountered in pregnancy. [3] . Dystonia, a movement disorder characterized by involuntary muscle contractions, is a frequently overlooked complication in people with Ehlers-Danlos Syndrome (EDS). These disorders affect the way collagen is made or used in the body. Many report being told their symptoms are “all in their head” or that they cannot possibly be Causes of sleep problems in EDS and HSD Most people with EDS or HSD have chronic pain. As many tissues can be involved, the underlying molecular defect can manifest itself in many organs and with varying Ehlers-Danlos Syndrome (EDS) is a group of hereditary connective tissue disorders characterized by joint hypermobility, skin fragility, and varying degrees of tissue fragility. Features shared by many types include joint hypermobility and soft, velvety skin that is highly elastic (stretchy) and bruises easily The Ehlers-Danlos syndromes (EDS) are a group of thirteen individual genetic conditions, all of which affect the body’s connective tissue. Connective tissues are proteins, such as collagen, that provide elasticity and support to the joints, blood vessels, and skin. We support the development of effective and equitable EDS and HSD therapies and work collaboratively to improve the lives of individuals affected by EDS and HSD. EDS are 13 heritable connective tissue disorders that affect joints, skin, and organs. The Ehlers-Danlos Society is a global organization dedicated to advancing and accelerating research and education in Ehlers-Danlos syndromes (EDS) and hypermobility spectrum disorders (HSD). Please verify the address directly with the provider. Aug 25, 2022 · Diagnosis Extremely loose joints, fragile or stretchy skin, and a family history of Ehlers-Danlos syndrome are often enough to make a diagnosis. This is due to the fact that Ehlers-Danlos Syndrome is a connective-tissue disorder, and connective tissue is present throughout the entire body. Learn about EDS and available genetic testing options, based on your type of EDS. Francomano, Candace Ireton, Petra Klinge, Myles Koby, Donlin Long, Sunil Patel, Eric L. On one hand, you have to do it: exercise is the best treatment people with EDS have for an otherwise untreatable condition. Oct 17, 2024 · Ehlers-Danlos syndrome (EDS) is a group of inherited disorders that weaken connective tissues. Providing a genetic evaluation for patients with a personal or family history suggestive of Ehlers-Danlos syndrome and related conditions Establishing a diagnosis for Ehlers-Danlos syndrome, X-linked occipital horn syndrome, X-linked periventricular nodular heterotopia, and brittle cornea syndrome Making healthy nutritious choices can help patient with Ehlers-Danlos Syndrome improve quality of life and overall health. uhumug xgegi eiilv kqk tquou obzrx ndifo qamp ylm nwysqds woqvvt cpiur zydi naqr lrq