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...

Full description

Saved in:
Bibliographic Details
Main Authors: Imran Uddin, Rafat Jan
Format: Article
Language:English
Published: Liaquat University of Medical and Health Sciences 2024-12-01
Series:Liaquat Medical Research Journal
Subjects:
Online Access:http://121.52.154.206:80/index.php/LMRJ/article/view/1185
Tags: Add Tag
No Tags, Be the first to tag this record!