Diagnostic Approach in Cystinuria: A Case Report
Cystinuria is an, inherited metabolic disorder progressing with recurrent kidney stones due to impaired reabsorption of dibasic amino acids and arises from mutations in the SLC3A1 and SLC7A9 on chromosome 2. Cystine crystals were detected in the urinalysis of a 17-year-old male patient who was inve...
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| Main Authors: | , , |
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| Format: | Article |
| Language: | English |
| Published: |
Aydın Pediatric Society
2021-06-01
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| Series: | Trends in Pediatrics |
| Subjects: | |
| Online Access: | https://trendspediatrics.com/article/view/29 |
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