A Case Report About One Patient with Citrullinemia Type I with Classic Bartter Syndrome Simultaneously

Abstract

Introduction and Case Presentation: This report describes a 9-year-old child diagnosed simultaneously with two rare metabolic and nephrogenic disorders. The diagnosis followed non-specific symptoms that began in early infancy and were further investigated through laboratory results. Conclusions: Each of these disorders requires independent treatment and care. Therefore, it was essential for the patient to receive training on recognizing warning signs.