Ehlers-Danlos Support UK - Hypermobility Ehlers-Danlos syndrome (also known as EDS-HT and previously known as HEDS and EDS type 3) is the most prevalent form of EDS. The terminology used by healthcare
![Hypermobile Ehlers‐Danlos syndromes: Complex phenotypes, challenging diagnoses, and poorly understood causes - Gensemer - 2021 - Developmental Dynamics - Wiley Online Library Hypermobile Ehlers‐Danlos syndromes: Complex phenotypes, challenging diagnoses, and poorly understood causes - Gensemer - 2021 - Developmental Dynamics - Wiley Online Library](https://anatomypubs.onlinelibrary.wiley.com/cms/asset/e0c26b32-a160-46f0-b077-01a41461b57b/dvdy.v250.3.cover.jpg)
Hypermobile Ehlers‐Danlos syndromes: Complex phenotypes, challenging diagnoses, and poorly understood causes - Gensemer - 2021 - Developmental Dynamics - Wiley Online Library
![Deciphering disease signatures and molecular targets in vascular Ehlers- Danlos syndrome through transcriptome and miRNome sequencing of dermal fibroblasts - ScienceDirect Deciphering disease signatures and molecular targets in vascular Ehlers- Danlos syndrome through transcriptome and miRNome sequencing of dermal fibroblasts - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0925443923002818-ga1.jpg)
Deciphering disease signatures and molecular targets in vascular Ehlers- Danlos syndrome through transcriptome and miRNome sequencing of dermal fibroblasts - ScienceDirect
![Genes | Free Full-Text | Cellular and Molecular Mechanisms in the Pathogenesis of Classical, Vascular, and Hypermobile Ehlers‒Danlos Syndromes Genes | Free Full-Text | Cellular and Molecular Mechanisms in the Pathogenesis of Classical, Vascular, and Hypermobile Ehlers‒Danlos Syndromes](https://www.mdpi.com/genes/genes-10-00609/article_deploy/html/images/genes-10-00609-g001.png)
Genes | Free Full-Text | Cellular and Molecular Mechanisms in the Pathogenesis of Classical, Vascular, and Hypermobile Ehlers‒Danlos Syndromes
![Beyond bones: The relevance of variants of connective tissue (hypermobility) to fibromyalgia, ME/CFS and controversies surrounding diagnostic classification: an observational study | RCP Journals Beyond bones: The relevance of variants of connective tissue (hypermobility) to fibromyalgia, ME/CFS and controversies surrounding diagnostic classification: an observational study | RCP Journals](https://www.rcpjournals.org/content/clinmedicine/21/1/53/F1.large.jpg)
Beyond bones: The relevance of variants of connective tissue (hypermobility) to fibromyalgia, ME/CFS and controversies surrounding diagnostic classification: an observational study | RCP Journals
![Frontiers | The Role of Cell Adhesion and Cytoskeleton Dynamics in the Pathogenesis of the Ehlers-Danlos Syndromes and Hypermobility Spectrum Disorders Frontiers | The Role of Cell Adhesion and Cytoskeleton Dynamics in the Pathogenesis of the Ehlers-Danlos Syndromes and Hypermobility Spectrum Disorders](https://www.frontiersin.org/files/Articles/649082/fcell-09-649082-HTML/image_m/fcell-09-649082-g004.jpg)
Frontiers | The Role of Cell Adhesion and Cytoskeleton Dynamics in the Pathogenesis of the Ehlers-Danlos Syndromes and Hypermobility Spectrum Disorders
![Understanding the Association of Ehlers Danlos Syndrome and Chronic Inflammatory Response Syndrome - The ID Doc Understanding the Association of Ehlers Danlos Syndrome and Chronic Inflammatory Response Syndrome - The ID Doc](https://www.theiddoc.com/wp-content/uploads/2021/01/Mast-Cell-Activation-Disorder-and-Ehlers-Danlos-Syndrome.png)
Understanding the Association of Ehlers Danlos Syndrome and Chronic Inflammatory Response Syndrome - The ID Doc
![Biological insights in the pathogenesis of hypermobile Ehlers-Danlos syndrome from proteome profiling of patients' dermal myofibroblasts - ScienceDirect Biological insights in the pathogenesis of hypermobile Ehlers-Danlos syndrome from proteome profiling of patients' dermal myofibroblasts - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0925443920303999-gr1.jpg)
Biological insights in the pathogenesis of hypermobile Ehlers-Danlos syndrome from proteome profiling of patients' dermal myofibroblasts - ScienceDirect
![Multisystemic manifestations in a cohort of 75 classical Ehlers-Danlos syndrome patients: natural history and nosological perspectives | Orphanet Journal of Rare Diseases | Full Text Multisystemic manifestations in a cohort of 75 classical Ehlers-Danlos syndrome patients: natural history and nosological perspectives | Orphanet Journal of Rare Diseases | Full Text](https://media.springernature.com/lw685/springer-static/image/art%3A10.1186%2Fs13023-020-01470-0/MediaObjects/13023_2020_1470_Fig4_HTML.png)
Multisystemic manifestations in a cohort of 75 classical Ehlers-Danlos syndrome patients: natural history and nosological perspectives | Orphanet Journal of Rare Diseases | Full Text
![Cells | Free Full-Text | RNA-Seq of Dermal Fibroblasts from Patients with Hypermobile Ehlers–Danlos Syndrome and Hypermobility Spectrum Disorders Supports Their Categorization as a Single Entity with Involvement of Extracellular Matrix Degrading Cells | Free Full-Text | RNA-Seq of Dermal Fibroblasts from Patients with Hypermobile Ehlers–Danlos Syndrome and Hypermobility Spectrum Disorders Supports Their Categorization as a Single Entity with Involvement of Extracellular Matrix Degrading](https://pub.mdpi-res.com/cells/cells-11-04040/article_deploy/html/images/cells-11-04040-g006.png?1671170119)
Cells | Free Full-Text | RNA-Seq of Dermal Fibroblasts from Patients with Hypermobile Ehlers–Danlos Syndrome and Hypermobility Spectrum Disorders Supports Their Categorization as a Single Entity with Involvement of Extracellular Matrix Degrading
![Ehlers-Danlos syndrome hypermobility type is associated with rheumatic diseases | Scientific Reports Ehlers-Danlos syndrome hypermobility type is associated with rheumatic diseases | Scientific Reports](https://media.springernature.com/full/springer-static/image/art%3A10.1038%2Fsrep39636/MediaObjects/41598_2017_Article_BFsrep39636_Fig1_HTML.jpg)
Ehlers-Danlos syndrome hypermobility type is associated with rheumatic diseases | Scientific Reports
![Biological insights in the pathogenesis of hypermobile Ehlers-Danlos syndrome from proteome profiling of patients' dermal myofibroblasts - ScienceDirect Biological insights in the pathogenesis of hypermobile Ehlers-Danlos syndrome from proteome profiling of patients' dermal myofibroblasts - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0925443920303999-ga1.jpg)
Biological insights in the pathogenesis of hypermobile Ehlers-Danlos syndrome from proteome profiling of patients' dermal myofibroblasts - ScienceDirect
![Cells | Free Full-Text | RNA-Seq of Dermal Fibroblasts from Patients with Hypermobile Ehlers–Danlos Syndrome and Hypermobility Spectrum Disorders Supports Their Categorization as a Single Entity with Involvement of Extracellular Matrix Degrading Cells | Free Full-Text | RNA-Seq of Dermal Fibroblasts from Patients with Hypermobile Ehlers–Danlos Syndrome and Hypermobility Spectrum Disorders Supports Their Categorization as a Single Entity with Involvement of Extracellular Matrix Degrading](https://www.mdpi.com/cells/cells-11-04040/article_deploy/html/images/cells-11-04040-g001-550.jpg)
Cells | Free Full-Text | RNA-Seq of Dermal Fibroblasts from Patients with Hypermobile Ehlers–Danlos Syndrome and Hypermobility Spectrum Disorders Supports Their Categorization as a Single Entity with Involvement of Extracellular Matrix Degrading
![Schematic illustration summarizing the processes likely involved in the... | Download Scientific Diagram Schematic illustration summarizing the processes likely involved in the... | Download Scientific Diagram](https://www.researchgate.net/publication/335139137/figure/fig1/AS:791419606294530@1565700546332/Schematic-illustration-summarizing-the-processes-likely-involved-in-the-pathogenesis-of.jpg)
Schematic illustration summarizing the processes likely involved in the... | Download Scientific Diagram
The Ehlers-Danlos Society - Hypermobile EDS is an inherited condition and different people often experience different symptoms, even within the same family. However, many common hEDS symptoms are very similar to those
![Multisystemic manifestations in a cohort of 75 classical Ehlers-Danlos syndrome patients: natural history and nosological perspectives | Orphanet Journal of Rare Diseases | Full Text Multisystemic manifestations in a cohort of 75 classical Ehlers-Danlos syndrome patients: natural history and nosological perspectives | Orphanet Journal of Rare Diseases | Full Text](https://media.springernature.com/lw685/springer-static/image/art%3A10.1186%2Fs13023-020-01470-0/MediaObjects/13023_2020_1470_Fig3_HTML.png)