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Scientists hunt for missing genes behind rare blood disorder

NCT ID NCT07459816

First seen Mar 22, 2026 · Last updated Jun 18, 2026 · Updated 15 times

Summary

This study looks for new genetic causes of congenital sideroblastic anemias, a group of rare blood disorders where the body cannot properly use iron to make red blood cells. Researchers will analyze DNA from 20 people whose genetic cause is still unknown. The goal is to find and confirm new genes involved in this condition.

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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: •••••@•••••

Locations

  • Amiens University Hospital

    RECRUITING

    Amiens, 80054, France

Conditions

The condition(s) this trial relates to.

anemia autosomal recessive sideroblastic anemia

As listed by the trial registrant

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