Scientists map rare skin disease to unlock future treatments
NCT ID NCT02081313
First seen Dec 10, 2025 · Last updated May 23, 2026 · Updated 23 times
Summary
This study followed 18 people with Netherton syndrome, a rare genetic skin disorder, to learn how the disease affects the body over time. Researchers measured immune system markers and skin changes to better understand the condition. No new treatments were tested; the goal was to gather knowledge that could lead to future therapies.
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Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
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Locations
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Imagine Institute for genetic diseases
Paris, 75015, France
Conditions
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