Scientists hunt for genes behind rare lung complication in liver shunt patients
NCT ID NCT07314814
First seen Jan 11, 2026 · Last updated May 13, 2026 · Updated 21 times
Summary
This study aims to find genetic changes in people who have both a rare liver blood vessel problem (congenital portosystemic shunt) and a serious lung condition called portopulmonary hypertension. Researchers will analyze DNA from 120 patients and their close family members to identify genes that may increase risk. The goal is to use this information to predict and manage the lung condition earlier in at-risk patients.
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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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University Hospitals Geneva / University of Geneva
Geneva, Canton of Geneva, 1205, Switzerland
Conditions
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