Unveiling the complexities: A case report on complications arising from propionic acidemia
Propionic acidemia is a rare inherited metabolic disorder caused by a defect in propionyl-coenzyme A (CoA) carboxylase, resulting in the accumulation of propionic acid. We present a case involving a 5-year-old male with a known history of propionic acidemia who presented to the emergency department...
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| Main Authors: | Imran Uddin, Rafat Jan |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Liaquat University of Medical and Health Sciences
2024-12-01
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| Series: | Liaquat Medical Research Journal |
| Subjects: | |
| Online Access: | http://121.52.154.206:80/index.php/LMRJ/article/view/1185 |
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