Registry for men with CAH (21-hydroxylase deficiency)
Part of Genetic & congenital, Hormones & metabolism, Kidney & urinary, Women’s health & pregnancy clinical trials.
This trial is creating a registry to track adult males with congenital adrenal hyperplasia (CAH) from 21-hydroxylase deficiency. It helps doctors learn more about the condition and how it changes over time.
Summary written for real people, not researchers, by Clin2.
Who can take part
- You identify as male.
- You are at least 18 years old.
- You have been diagnosed with congenital adrenal hyperplasia (CAH) caused by 21-hydroxylase deficiency.
- You have already had a genetic test (CYP21A2 gene analysis) that found the specific mutation causing your CAH.
- You are willing to sign a consent form agreeing to join the registry.
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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