HEREDITARY CHRONIC PANCREATITIS: CLINICAL EXOME PANEL (Sec. & CNVs) – 11 genes
Delivery time
3-4 weeks
Sample
Blood
850,00€
The Hereditary Chronic Pancreatitis panel analyzes 11 genes involved in the genetic predisposition to recurrent or chronic pancreatitis. Using next-generation sequencing (NGS) with detection of SNVs, indels, and CNVs, it identifies alterations that affect trypsin activation, pancreatic secretion, and ductal function. Its analysis facilitates etiological diagnosis, prediction of the risk of pancreatic insufficiency or diabetes, and identification of familial carriers, guiding preventive measures and clinical follow-up. Genes included: APOA5, APOC2, CASR, CFTR, CPA1, CTRC, GPIHBP1, PRSS1, SBDS, SPINK1, UBR1.
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