Registry for people with atypical hemolytic uremic syndrome
Part of Blood & lymphatic, Kidney & urinary, Women’s health & pregnancy clinical trials.
This is a registry that collects information from people diagnosed with atypical hemolytic uremic syndrome (aHUS). It helps researchers better understand the condition across different genetic causes and treatment needs.
Summary written for real people, not researchers, by Clin2.
Who can take part
- You must have a diagnosis of aHUS (at any age, including children).
- It can be with or without a known complement gene change (or related blood antibodies).
- You (or your parent/legal guardian for a child) must be able and willing to sign consent forms.
- If you are a minor, you must be willing to give assent (agreement) when required.
- If a test is done, your ADAMTS13 result must be more than 5%.
Quick eligibility check
Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.
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