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Ehlers-Danlos syndrome

American  
[ey-lerz dan-los, -luhs] / ˈeɪ lərz ˈdæn lɒs, -ləs /

noun

Pathology.
  1. a rare hereditary disease of connective tissue, characterized by joint hypermotility and abnormally stretchable skin.


Etymology

Origin of Ehlers-Danlos syndrome

After Edvard Ehlers (1863–1937), Danish dermatologist, and Henri Alexandre Danlos (1844–1912), French dermatologist, who separately reported it in 1901 and 1908

Example Sentences

Examples are provided to illustrate real-world usage of words in context. Any opinions expressed do not reflect the views of Dictionary.com.

See Examples For:

Ritchie has Ehlers-Danlos syndrome, a condition that affects the joints; functional neurological disorder, which impacts her mobility; Addison's disease, a hormonal disorder, and epilepsy.

From BBC Feb. 24, 2026

One condition she points to is hypermobile Ehlers-Danlos syndrome, or hEDS, in which a person’s joints have an unusually large range of movement.

From Salon May 13, 2025

She was also diagnosed with Ehlers-Danlos syndrome, a connective tissue disorder, which she thinks was overlooked when her body pains were categorized as a psychosomatic outgrowth of bipolar.

From Slate Sep. 29, 2024

Some inherited disorders, like Marfan syndrome and Ehlers-Danlos syndrome, may increase a person’s chances of developing an aortic aneurysm.

From New York Times Dec. 14, 2022

In 2017, she was diagnosed with hypermobile Ehlers-Danlos syndrome, a connective tissue disorder often causing loose joints, dislocations and chronic pain.

From Washington Post

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