Hidden gene behind breathlessness? new study investigates
NCT ID NCT07152834
First seen Nov 01, 2025 · Last updated May 22, 2026 · Updated 31 times
Summary
This study looks at whether a genetic condition called Alpha-1 Antitrypsin Deficiency (AATD) is more common in people who have shortness of breath and signs of airway blockage. Researchers will test blood samples from 734 adults to measure AAT protein levels and check for related gene mutations. The goal is to find undiagnosed cases and improve detection of this treatable lung condition.
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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.
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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Study contacts
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Contact
Phone: •••-•••-•••• Email: •••••@•••••
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Contact
Phone: •••-•••-•••• Email: •••••@•••••
Locations
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Muğla Training and Research Hospital
RECRUITINGMuğla, Menteşe, 48000, Turkey (Türkiye)
Contact
Contact
Contact Phone: •••-•••-•••• Email: •••••@•••••
Conditions
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