Version May 2024
| Diagnosis | Joint hypermobility | Other features suggestive of a connective tissue disorder* | Musculoskeletal complications¶ |
| Hypermobile Ehlers-Danlos syndrome (hEDS) | Yes, must be generalized | Yes, refer to 2017 international criteria for hypermobile Ehlers-Danlos syndrome*[1] | Yes in most patientsΔ |
| Hypermobility spectrum disorder (HSD) | Yes, may be generalized, local/regional, or peripheral (small joints) | No | Yes |
* Including skin findings, Marfanoid features, and family history of hEDS in the absence of other heritable and acquired connective tissue disorders. Refer to UpToDate content on clinical manifestations and diagnosis of hEDS and HSD for a full description of criteria.
¶ Including recurrent musculoskeletal pain, diffuse widespread pain, and recurrent atraumatic joint dislocations or joint instability. Refer to UpToDate content on clinical manifestations and diagnosis of hEDS and HSD for more information.
Δ Patients may still be diagnosed with hEDS in the absence of musculoskeletal complications. Refer to UpToDate content on clinical manifestations and diagnosis of hEDS and HSD for a full description of criteria.آیا می خواهید مدیلیب را به صفحه اصلی خود اضافه کنید؟
