Volume 9, Issue 1 (2-2020)
aumj 2020, 9(1): 91-94 |
Back to browse issues page
Download citation:
BibTeX | RIS | EndNote | Medlars | ProCite | Reference Manager | RefWorks
Send citation to:
BibTeX | RIS | EndNote | Medlars | ProCite | Reference Manager | RefWorks
Send citation to:
Yaghmaie B, Sayarifard F, Noohi A H. Glutaric Aciduri Type II, with Rhabdomyolysis and Acute Renal Failure Presentation in 10 Years Old Girl. aumj 2020; 9 (1) :91-94
URL: http://aums.abzums.ac.ir/article-1-1064-en.html
URL: http://aums.abzums.ac.ir/article-1-1064-en.html
1- Pediatric Intensivist, Children’s Medical Center, Tehran University of Medical Science, Tehran, Iran , byaghmaie@tums.ac.ir
2- Growth and Development Research Center, Children’s Medical Center, Tehran University of Medical Science, Tehran, Iran
3- Pediatric Intensivist, Imam Ali Hospital, Alborz University of Medical Sciences, Karaj, Iran
2- Growth and Development Research Center, Children’s Medical Center, Tehran University of Medical Science, Tehran, Iran
3- Pediatric Intensivist, Imam Ali Hospital, Alborz University of Medical Sciences, Karaj, Iran
Abstract: (2853 Views)
Introduction: Myopathy and rhabdomyolysis are not common in children and, if not detected and do not treated it will be associated with high mortality and morbidity rate.
The causes of rhabdomyolysis include hypokalemia, trauma, viral myositis, poisoning, rheumatoid diseases, and metabolic myopathies.
Rhabdomyolysis treatment includes rapid supportive care and treatment of the underlying disease leading to rhabdomyolysis.
Case Presentation: 10-year-old girl with progressive muscle weakness was admitted in Pediatric Intensive Care Unit (PICU) with acute renal failure and respiratory failure. The laboratory results showed myoglobinuria, high CPK, LDH.
The initial diagnosis was severe rhabdomyolysis. In addition to fluid therapy and diuretic, she was treated with carnitine and riboflavin with possible glutaric aciduria type II. The patient showed progressive improvement after a few days. Result of plasma acyl carnitine and urine organic acid analysis stablished the diagnosis of glutaric aciduria type II.
Conclusion
Late onset glutaric aciduria type II has been described as a rare but treatable cause of myopathy and rhabdomyolysis. Glutaric aciduria type II is an important differential diagnosis to consider in children and adults presenting with myopathy and rhabdomyolysis.
The causes of rhabdomyolysis include hypokalemia, trauma, viral myositis, poisoning, rheumatoid diseases, and metabolic myopathies.
Rhabdomyolysis treatment includes rapid supportive care and treatment of the underlying disease leading to rhabdomyolysis.
Case Presentation: 10-year-old girl with progressive muscle weakness was admitted in Pediatric Intensive Care Unit (PICU) with acute renal failure and respiratory failure. The laboratory results showed myoglobinuria, high CPK, LDH.
The initial diagnosis was severe rhabdomyolysis. In addition to fluid therapy and diuretic, she was treated with carnitine and riboflavin with possible glutaric aciduria type II. The patient showed progressive improvement after a few days. Result of plasma acyl carnitine and urine organic acid analysis stablished the diagnosis of glutaric aciduria type II.
Conclusion
Late onset glutaric aciduria type II has been described as a rare but treatable cause of myopathy and rhabdomyolysis. Glutaric aciduria type II is an important differential diagnosis to consider in children and adults presenting with myopathy and rhabdomyolysis.
Type of Study: Case Report |
Subject:
Special
Received: 2020/03/05 | Accepted: 2020/03/05 | Published: 2020/03/05
Received: 2020/03/05 | Accepted: 2020/03/05 | Published: 2020/03/05
Send email to the article author
| Rights and permissions | |
 |
This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License. |
