U.S., Feb. 18 -- ClinicalTrials.gov registry received information related to the study (NCT07413029) titled 'French National Cohort of Patients With PRSS1 Mutations' on Feb. 02.
Brief Summary: The diagnosis of hereditary pancreatitis (PH) is based on a genetic criterion - detection of a mutation in the PRSS1 gene or on a genealogical criterion - the presence of chronic pancreatitis in at least 2 first-degree relatives or at least 3 relatives in the second degree, in the absence of other identified predisposing factors (notably chronic alcohol consumption). It is now recommended to seek PH in cases of pancreatitis of unknown origin in a young patient or with a family history.
In this study, patients carrying a PRSS1 mutation will be identi...