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New study aims to uncover genetic roots of childhood birth defects and delays

NCT ID NCT07167017

First seen Nov 01, 2025 · Last updated Jun 22, 2026 · Updated 34 times

Summary

This study will look at genetic test results (karyotyping) from 75 children aged 1 month to 12 years who have birth defects and developmental delays. Researchers will collect medical history, do physical exams, and assess development to find out what types of chromosome changes cause these conditions. The goal is to better understand the genetic causes and identify families who may need further testing.

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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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Contacts and locations

Study contacts

  • Contact

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

  • Contact

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

Conditions

The condition(s) this trial relates to.

Congenital Abnormalities learning disability

As listed by the trial registrant

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