a case report about one patient with citrullinemia type i with classic bartter syndrome simultaneously

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.