![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. : r/Hypermobility 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. : r/Hypermobility](https://preview.redd.it/l0b0l592xac61.jpg?width=640&crop=smart&auto=webp&s=62c2fb41984398f734702e94610e4c64fc7dad1d)
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. : r/Hypermobility
![Familial EhlersDanlos syndrome in the son (a-d), the daughter (e), and... | Download Scientific Diagram Familial EhlersDanlos syndrome in the son (a-d), the daughter (e), and... | Download Scientific Diagram](https://www.researchgate.net/publication/318166925/figure/fig2/AS:738236968210439@1553020817948/Familial-EhlersDanlos-syndrome-in-the-son-a-d-the-daughter-e-and-the-father-f-h.jpg)
Familial EhlersDanlos syndrome in the son (a-d), the daughter (e), and... | Download Scientific Diagram
![PDF] Fibulin-5 mutations link inherited neuropathies, age-related macular degeneration and hyperelastic skin. | Semantic Scholar PDF] Fibulin-5 mutations link inherited neuropathies, age-related macular degeneration and hyperelastic skin. | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/6efb4bedc2470d1ec9f1ad4dcec5dac757493a37/8-Figure4-1.png)
PDF] Fibulin-5 mutations link inherited neuropathies, age-related macular degeneration and hyperelastic skin. | Semantic Scholar
![Family with Ehlers–Danlos syndrome (combined classic and vascular type) with rare presentation of progressive myopathy and unusual association of severe facial and trigeminal motor weakness Family with Ehlers–Danlos syndrome (combined classic and vascular type) with rare presentation of progressive myopathy and unusual association of severe facial and trigeminal motor weakness](https://neurologyindia.com/articles/2017/65/3/images/ni_2017_65_3_561_205933_f1.jpg)
Family with Ehlers–Danlos syndrome (combined classic and vascular type) with rare presentation of progressive myopathy and unusual association of severe facial and trigeminal motor weakness
![Recurrent venous thrombosis in Ehlers-Danlos syndrome type III: an atypical manifestation | BMJ Case Reports Recurrent venous thrombosis in Ehlers-Danlos syndrome type III: an atypical manifestation | BMJ Case Reports](https://casereports.bmj.com/content/casereports/2013/bcr-2013-008922/F1.large.jpg)
Recurrent venous thrombosis in Ehlers-Danlos syndrome type III: an atypical manifestation | BMJ Case Reports
![Pediatric Dermatology : Ehlers Danlos Syndrome : Ehlers Danlos Syndrome Patient Education : Diseases and Conditions | Pediatric Oncall Pediatric Dermatology : Ehlers Danlos Syndrome : Ehlers Danlos Syndrome Patient Education : Diseases and Conditions | Pediatric Oncall](https://www.pediatriconcall.com/master/bucket-img/130-ehlers-danlos-syndrome/ehlers-danlos-syndrome-1.jpg)
Pediatric Dermatology : Ehlers Danlos Syndrome : Ehlers Danlos Syndrome Patient Education : Diseases and Conditions | Pediatric Oncall
![Idiopathic osteoporosis, Ehlers–Danlos syndrome, postural orthostatic tachycardia syndrome, and mast cell activation disorder in a 27‐year‐old male patient: A unique case presentation - Rattray - 2022 - Clinical Case Reports - Wiley Online Library Idiopathic osteoporosis, Ehlers–Danlos syndrome, postural orthostatic tachycardia syndrome, and mast cell activation disorder in a 27‐year‐old male patient: A unique case presentation - Rattray - 2022 - Clinical Case Reports - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/fbc85ebe-505f-42a6-bac6-bc287a683c99/ccr35887-fig-0001-m.jpg)