![Clinical and molecular characterization of 40 patients with classic Ehlers–Danlos syndrome: identification of 18 COL5A1 and 2 COL5A2 novel mutations | Orphanet Journal of Rare Diseases | Full Text Clinical and molecular characterization of 40 patients with classic Ehlers–Danlos syndrome: identification of 18 COL5A1 and 2 COL5A2 novel mutations | Orphanet Journal of Rare Diseases | Full Text](https://media.springernature.com/full/springer-static/image/art%3A10.1186%2F1750-1172-8-58/MediaObjects/13023_2013_Article_564_Fig2_HTML.jpg)
Clinical and molecular characterization of 40 patients with classic Ehlers–Danlos syndrome: identification of 18 COL5A1 and 2 COL5A2 novel mutations | Orphanet Journal of Rare Diseases | Full Text
![Skin Manifestations, Multiple Aneurysms, and Carotid-Cavernous Fistula in Ehlers-Danlos Syndrome Type IV | Circulation Skin Manifestations, Multiple Aneurysms, and Carotid-Cavernous Fistula in Ehlers-Danlos Syndrome Type IV | Circulation](https://www.ahajournals.org/cms/asset/1fe9e149-0b1b-414e-bda9-4ca3e438fb3c/hc3893088001.jpeg)
Skin Manifestations, Multiple Aneurysms, and Carotid-Cavernous Fistula in Ehlers-Danlos Syndrome Type IV | Circulation
![Examples of cutaneous and articular manifestations of Ehlers-Danlos... | Download Scientific Diagram Examples of cutaneous and articular manifestations of Ehlers-Danlos... | Download Scientific Diagram](https://www.researchgate.net/publication/271596334/figure/fig1/AS:295135511367701@1447377197863/Examples-of-cutaneous-and-articular-manifestations-of-Ehlers-Danlos-syndrome-EDS.png)
Examples of cutaneous and articular manifestations of Ehlers-Danlos... | Download Scientific Diagram
![Systemic Multiple Aneurysms Caused by Vascular Ehlers-Danlos Syndrome - Xinyu Gui, Fangda Li, Lingeer Wu, Yuehong Zheng, 2016 Systemic Multiple Aneurysms Caused by Vascular Ehlers-Danlos Syndrome - Xinyu Gui, Fangda Li, Lingeer Wu, Yuehong Zheng, 2016](https://journals.sagepub.com/cms/10.1177/1538574416647501/asset/images/large/10.1177_1538574416647501-fig2.jpeg)
Systemic Multiple Aneurysms Caused by Vascular Ehlers-Danlos Syndrome - Xinyu Gui, Fangda Li, Lingeer Wu, Yuehong Zheng, 2016
![Frontiers | Case report: Mild phenotype of a patient with vascular Ehlers–Danlos syndrome and COL3A1 duplication mutation without alteration in the [Gly-X-Y] repeat sequence Frontiers | Case report: Mild phenotype of a patient with vascular Ehlers–Danlos syndrome and COL3A1 duplication mutation without alteration in the [Gly-X-Y] repeat sequence](https://www.frontiersin.org/files/Articles/1017446/fgene-13-1017446-HTML-r1/image_m/fgene-13-1017446-g001.jpg)
Frontiers | Case report: Mild phenotype of a patient with vascular Ehlers–Danlos syndrome and COL3A1 duplication mutation without alteration in the [Gly-X-Y] repeat sequence
Understanding hypermobile Ehlers-Danlos, & hypermobility spectrum disorder - This week, we're looking at features of the skin in hEDS. Manifestations that can arise include stretch marks, piezogenic papules, hyperextensibility, and atrophic scarring.
![Classical-like Ehlers–Danlos syndrome: a clinical description of 20 newly identified individuals with evidence of tissue fragility | Genetics in Medicine Classical-like Ehlers–Danlos syndrome: a clinical description of 20 newly identified individuals with evidence of tissue fragility | Genetics in Medicine](https://media.springernature.com/full/springer-static/image/art%3A10.1038%2Fs41436-020-0850-1/MediaObjects/41436_2020_850_Fig1_HTML.png)
Classical-like Ehlers–Danlos syndrome: a clinical description of 20 newly identified individuals with evidence of tissue fragility | Genetics in Medicine
![Ehlers-Danlos Syndrome, Hypermobility Type: An Underdiagnosed Hereditary Connective Tissue Disorder with Mucocutaneous, Articular, and Systemic Manifestations Ehlers-Danlos Syndrome, Hypermobility Type: An Underdiagnosed Hereditary Connective Tissue Disorder with Mucocutaneous, Articular, and Systemic Manifestations](https://static.hindawi.com/articles/isrn/volume-2012/751768/figures/751768.fig.001b.jpg)
Ehlers-Danlos Syndrome, Hypermobility Type: An Underdiagnosed Hereditary Connective Tissue Disorder with Mucocutaneous, Articular, and Systemic Manifestations
![A floppy infant without lingual frenulum and kyphoscoliosis: Ehlers Danlos syndrome case report | Italian Journal of Pediatrics | Full Text A floppy infant without lingual frenulum and kyphoscoliosis: Ehlers Danlos syndrome case report | Italian Journal of Pediatrics | Full Text](https://media.springernature.com/lw685/springer-static/image/art%3A10.1186%2Fs13052-021-00984-y/MediaObjects/13052_2021_984_Fig1_HTML.png)
A floppy infant without lingual frenulum and kyphoscoliosis: Ehlers Danlos syndrome case report | Italian Journal of Pediatrics | Full Text
![Genes | Free Full-Text | The Ehlers–Danlos Syndromes against the Backdrop of Inborn Errors of Metabolism Genes | Free Full-Text | The Ehlers–Danlos Syndromes against the Backdrop of Inborn Errors of Metabolism](https://www.mdpi.com/genes/genes-13-00265/article_deploy/html/images/genes-13-00265-g001.png)
Genes | Free Full-Text | The Ehlers–Danlos Syndromes against the Backdrop of Inborn Errors of Metabolism
![a, b) An 8-year-old girl with Ehlers-Danlos syndrome showing marked... | Download Scientific Diagram a, b) An 8-year-old girl with Ehlers-Danlos syndrome showing marked... | Download Scientific Diagram](https://www.researchgate.net/publication/318166925/figure/fig5/AS:738236972408833@1553020818163/a-b-An-8-year-old-girl-with-Ehlers-Danlos-syndrome-showing-marked-scarring-of-the-skin.jpg)
a, b) An 8-year-old girl with Ehlers-Danlos syndrome showing marked... | Download Scientific Diagram
![Ehlers-Danlos Syndrome Related to Gastrointestinal Problems and Eating Disorders - Universitat Autònoma de Barcelona - UAB Barcelona Ehlers-Danlos Syndrome Related to Gastrointestinal Problems and Eating Disorders - Universitat Autònoma de Barcelona - UAB Barcelona](http://www.uab.cat/Imatge/466/639/sindrome-ehlers-danlos-wide-web.jpeg)