New study aims to catch nerve damage early in rare genetic disease
NCT ID NCT05311488
First seen Nov 01, 2025 · Last updated May 01, 2026 · Updated 31 times
Summary
This study tested different methods to detect early signs of nerve damage in people with hereditary transthyretin amyloidosis, a genetic condition that can cause nerve problems. Researchers compared blood tests, skin biopsies, and other exams in 47 participants over 12 months. The goal was to find the best way to spot nerve damage early, which could help doctors monitor the disease more effectively.
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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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University of Pennsylvania
Philadelphia, Pennsylvania, 19104, United States
Conditions
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