Blog

Now Online: Brussels Dupuytren Presentations

It’s here! Video presentations from the 2025 International Conference on Dupuytren Disease and Related Conditions are now online. This global summit is held every five years to showcase the latest developments in Dupuytren disease and related conditions and promote international collaboration toward better treatments. This year’s conference was the largest

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Running For Dupuytren Research

Running.    100 Miles.    Uphill.    In the Summer.    At 12,000 Feet. Daniel Kinek is an ultramarathon runner. He will run the Leadville 100-mile trail race on August 17, 2024, to raise awareness about Dupuytren Disease. Daniel doesn’t have Dupuytren, but his family does. He will be running a difficult 100 miles

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Dupuytren in the Family: What are the Odds?

  Dupuytren disease is genetic. It runs in families – but how? It depends on ancestry, age, gender, and relatives. Not everyone with Dupuytren has bent fingers. Dupuytren disease is any Dupuytren changes of the palms. Nodules, puckered skin, or cords are all signs of Dupuytren disease. Dupuytren contracture is Dupuytren disease

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Happy Birthday, Dupuytren, and Thanks for the Name!

Happy Dupuytren Day! Guillaume Dupuytren, the famous surgeon, was born on 5 October 1777. He would have been 246 years old today. If he were alive now, there’s a good chance he’d have the disease named after himself. Why is it called Dupuytren disease or Dupuytren contracture? Most medical disorders

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DNA, Drinks, and Dupuytren

While it’s estimated Dupuytren’s disease impacts over 10 million Americans, the current treatment options available to patients – mainly surgical procedures – are inadequate. Medicine has been focused on treating Dupuytren-related finger deformities rather than preventative measures or finding a cure at the biological level. Yet, with increasing recognition of

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