Cover Image, Volume 61, Number 4, April 2026

Key Points

• The aim is to explore the genetic variants associated with pseudo-Bartter syndrome in an infant with pancreatic insuficiency.
• Case report on an infant with pancreatic insufficiency and genetic variants in CFTR, DNAH9, LYST, and G6PD.
• Investigation of clinical symptoms and genetic testing results.
• Identification of CFTR, DNAH9, LYST, and G6PD variants in the patient.
• Clinical presentation consistent with pseudo-Bartter syndrome influenced by genetic factors.