ICD E25.0ORPHA:90794CAH

Congenital Adrenal Hyperplasia

Congenital adrenal hyperplasia is a group of inherited conditions affecting the adrenal glands, most commonly caused by 21-hydroxylase deficiency. It disrupts cortisol and aldosterone production and can cause virilisation. It is detected through newborn screening in Australia. Lifelong hormone replacement therapy is the cornerstone of management.

633
Articles
62
Trials (2 AU)
Updated
26 March 2026
Loading...

Common Questions

What is Congenital Adrenal Hyperplasia?

Congenital adrenal hyperplasia is a group of inherited conditions affecting the adrenal glands, most commonly caused by 21-hydroxylase deficiency. It disrupts cortisol and aldosterone production and can cause virilisation. It is detected through newborn screening in Australia. Lifelong hormone replacement therapy is the cornerstone of management.

How many clinical trials are available for Congenital Adrenal Hyperplasia?

RareWays currently indexes 62 clinical trials for Congenital Adrenal Hyperplasia, of which 13 are actively recruiting. Trial availability changes as new studies are registered — check the trials tab for current status.

Where does the research data for Congenital Adrenal Hyperplasia come from?

RareWays aggregates research from PubMed, Europe PMC, OpenAlex, and ClinicalTrials.gov. Data is updated regularly by Rocky, RareWays' automated research engine. All articles and trials link directly to their original sources.

Get research updates

Monthly email when new findings are published for Congenital Adrenal Hyperplasia.

No spam. Unsubscribe any time. Not medical advice.

This information is for general awareness only.

For guidance specific to your situation, please speak with your healthcare team.