Veds Hypermobility, There are 13 different types of EDS, but they do have some clinical features in common. At UVA Health EDS and Hypermobility Disorders Center, we provide personalized, multi-specialty care for adults and children with EDS and hypermobility spectrum disorders (HSD). What is skin hyperextensibility? May 20, 2025 · The hypermobile type of Ehlers-Danlos syndrome (hEDS) and hypermobility spectrum disorder (HSD) are among a group of conditions characterized by joint hypermobility and other frequently shared clinical features (table 1 and table 2). Consequently, individuals with EDS often experience symptoms such as joint hypermobility, skin hyperextensibility, and tissue fragility, which can vary significantly in severity and presentation. ligaments blood vessels internal organs and bones . g. 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. Comprehensive treatment for Ehlers-Danlos Syndrome and Hypermobility Spectrum Disorders If you are living with joint hypermobility, chronic pain, or mobility challenges due to Ehlers-Danlos Syndrome (EDS) or a hypermobility spectrum disorder (HSD), Casa Colina Hospital and Centers for Healthcare can help. Find out how hEDS is diagnosed and can be managed. EDS and Hypermobility Network Australia is a multidisciplinary team combining physiotherapy, general practice, integrative health, and movement-based rehabilitation supports improved diagnosis, management, and long-term outcomes for individuals with EDS, hEDS, and HSD across South Australia. Find out more about Hypermobile Ehlers-Danlos Syndrome using our easy to navigate body map. Select from the list below to learn how vEDS can affect the cardiovascular system. Hypermobile Ehlers-Danlos Syndrome (hEDS) What is hypermobile Ehlers-Danlos syndrome (hEDS)? hEDS is a heritable connective tissue disorder that causes generalized joint hypermobility, joint instability, and chronic pain. Ehlers-Danlos syndromes (EDS) are a group of rare inherited conditions that affect connective tissue. The clinical diagnosis of Vascular type Ehler-Danlos syndrome (Type IV EDS or vEDS) is suggested by a combination of thin skin, prominent veins, a susceptibility to bruising, a characteristic facial appearence and a history of organ rupture e. This page is intended to provide information about symptoms that may occur in individuals with vEDS and does not constitute medical advice. Hypermobile EDS is now understood as a multi-system disorder which can have a marked impact on health and which may help us to explain apparently mysterious multiple symptoms 4,5. other types of EDS, Loeys-Dietz syndrome, Marfan syndrome), and skeletal The old diagnosis of Joint Hypermobility syndrome (JHS) is now considered part of the spectrum of Hypermobile EDS 3. Although joint hypermobility is observed across all types of EDS, not everyone with a type of EDS has joint hypermobility. Alternative diagnoses and diagnostic categories include, but are not limited to, neuromuscular disorders (e. You can read more about joint hypermobility here. Unless otherwise stated, Mayo Clinic does not sponsor or endorse these websites, nor does Mayo Clinic guarantee the accuracy of the information contained on these websites. Find out about the symptoms, causes and treatments. uterine or gastrointestinal rupture. 1 day ago · What is Ehlers-Danlos syndrome? #doctor#eds#hypermobility#ehlersdanlos Dottie Steinbeck and Sara Filipczyk 2 Last viewed on: May 11, 2026 OCR: EHLERS-DANLOS SYNDROME Ehlers Danlos syndromes are a group of rare . Bethlem myopathy), other hereditary disorders of the connective tissue (e. Knight, Medical Director of the UVA Health EDS and Hypermobility Disorder Center, shares why hypermobile EDS (hEDS) is a serious condition even when not life-threatening, and why a negative genetic test doesn't rule out a diagnosis. These can include joint hypermobility, stretchy skin and tissue fragility. hEDS is also associated with a variety of other symptoms and related conditions that affect many different areas of the body. EDS ECHO Participant CORE Network Member International Consortium Member Manages vEDS Manages Rarer Types of EDS Offers Telehealth 2489 listings found • Sorted by last updated Joint hypermobility is observed throughout the body in most types of EDS, but hypermobility may be limited to the hands and feet in some types. Always consult a healthcare professional for personalized medical guidance. Exclusion of alternative diagnoses that may also include joint hypermobility by means of hypotonia and/or connective tissue laxity. it presents in different ways and in some people it can be . Aug 18, 2023 · We aim to review an unusual presentation of vascular EDS (vEDS) in a pediatric patient and further discuss the role of EDS as a differential diagnosis in children. Jul 10, 2021 · Yes, you may have EDS without hypermobility, especially in Vascular Ehlers-Danlos Syndrome. Resources Resources for patients with suspected hypermobility syndromes, including hypermobile Ehlers -Danlos syndrome (hEDS) and Hypermobile Syndrome Disorder (HSD). 3. Vascular EDS (vEDS) is a rare type of EDS. In vEDS, patients do not have extreme hypermobility (Very less only of toes and fingers) instead of common facial issues. 5 days ago · Dr. uhlpgkrhxb8asi9oinaox4ymiyyxlkvgrys73t6eswkycf4pmogkp8nc