Delayed Diagnosis of Crigler-Najjar Disease: A Case Report of a 17-Year-Old Man with Progressive Jaundice
Crigler-Najjar syndrome type II is a metabolic disorder stemming from mutations in the UGT1A1 gene, resulting in heightened levels of unconjugated bilirubin. Here is a case report of a 17-year-old male patient with minor thalassemia and G6PD deficiency who was referred due to worsening jaundice. He...
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| Huvudupphov: | , , , |
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| Materialtyp: | Artigo |
| Språk: | Inglês |
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Tehran University of Medical Sciences
2024-12-01
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| Serie: | Case Reports in Clinical Practice |
| Ämnen: | |
| Länkar: | https://crcp.tums.ac.ir/index.php/crcp/article/view/989 |
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