Heart defects and hidden genes: new study to reveal genetic links

NCT ID NCT07204509

First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study will examine 138 children with congenital heart disease to find out how many also have chromosomal abnormalities. Researchers will use a standard genetic test called karyotyping to look for missing or extra chromosomes. The goal is to improve diagnosis, treatment planning, and genetic counseling for families.

What this could mean

Our plain-language read of the trial. This is informational only — not medical advice or a prediction.

What this could lead to

If successful, this study could help doctors better understand which genetic changes are linked to heart defects, leading to earlier diagnosis and improved family counseling.

What could go wrong

This is an observational study that only looks at genetic patterns—it does not test a treatment. Results may not apply to all populations, and karyotyping may miss small genetic changes.

Disclaimer Read more

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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Conditions

The condition(s) this trial relates to.

chromosomal disorder Chromosome Aberrations congenital heart disease

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Study contacts

  • Contact

    Phone: •••-•••-•••• Email: •••••@•••••