Multiple cartilaginous outgrowth syndrome MHE
MHE is an inherited disease resulting from changes in the EXT1 or EXT2 gene. The cause of the mutation is still not identified. It mostly occurs in boys and develops as bone tissue grows.
The outgrowths are benign tumors that can develop into malignant tumors over time
You can learn more about it from our specialists Dr. J. Michal Deszczynski and Dr. Tomasz Albrewczynski and read in a recent article for Onet health: "There are days when we both cry... Hubert from pain, and I from helplessness. Multiple cartilaginous outgrowth (MHE) syndrome."
We also invite you to listen to Dr. Feldman's lecture:
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July 16, 2026
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The Paley European Institute Wins Two Awards in the “Patient Trust Leader 2026” Competition
It is with great joy and pride that we announce that the Paley European Institute has received the “Patient Trust Leader 2026” Quality Seal and the “Golden Laurel for Patient Care” Special Award in the National Quality Competition organized by the European Center for Quality Research. We received the awards during the ceremonial Final Gala, which took place on July 6, 2026, in Warsaw. This is a truly special moment for us […]