A Case Report About One Patient with Citrullinemia Type I with Classic Bartter Syndrome Simultaneously
| Author | Davood Amirkashani | en |
| Author | Samayeh Dadakhani | en |
| Orcid | Davood Amirkashani [0000-0002-0838-3005] | en |
| Orcid | Samayeh Dadakhani [0000-0001-7177-1783] | en |
| Issued Date | 2024-07-31 | en |
| 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. | en |
| DOI | https://doi.org/10.5812/zjrms-148271 | en |
| Keyword | Citrullinemia | en |
| Keyword | Bartter Syndrome | en |
| Keyword | Metabolic Disorders | en |
| Publisher | Brieflands | en |
| Title | A Case Report About One Patient with Citrullinemia Type I with Classic Bartter Syndrome Simultaneously | en |
| Type | Case Report | en |
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