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Literature DB >> 7161012

Myoglobinuria in carnitine palmityltransferase deficiency.

Abstract

An 18-year-old male developed recurrent myoglobinuria after prolonged physical exertion. Histochemical analysis of biopsied muscle revealed complete absence of carnitine palmityltransferase. Significant ultrastructural abnormalities of muscle were present, but these could be the result of the recent episode of rhabdomyolysis. Recurrent myoglobinuria can occur in several disorders of glycogen and lipid metabolism in muscle, and such disorders should be suspected in cases of unexplained recurrent myoglobinuria.

Entities: Chemical Disease

Mesh：

Substances：

Year: 1982 PMID： 7161012 DOI： 10.1007/bf02081815

Source DB: PubMed Journal: Int Urol Nephrol ISSN： 0301-1623 Impact factor: 2.370

23 in total

1. A disorder of muscle lipid metabolism and myoglobinuria. Absence of carnitine palmityl transferase.

Authors: W J Bank; S DiMauro; E Bonilla; D M Capuzzi; L P Rowland
Journal: N Engl J Med Date: 1975-02-27 Impact factor: 91.245

2. Myopathy due to a defect in muscle glycogen breakdown.

Authors: B McARDLE
Journal: Clin Sci Date: 1951-02 Impact factor: 6.124

3. Recurrent myoglobinuria and muscle carnitine palmityltransferase deficiency.

Authors: J Herman; H L Nadler
Journal: J Pediatr Date: 1977-08 Impact factor: 4.406

4. Muscle phosphofructokinase deficiency.

Authors: W E Tobin; F Huijing; R S Porro; R T Salzman
Journal: Arch Neurol Date: 1973-02

5. Exercise myoglobinemia and acute exertional rhabdomyolysis.

Authors: M A Demos; E L Gitin; L J Kagen
Journal: Arch Intern Med Date: 1974-10

6. Renal failure in McArdle's disease.

Authors: W J Bank; S DiMauro; L P Rowland
Journal: N Engl J Med Date: 1972-11-23 Impact factor: 91.245

7. Combined partial deficiency of muscle carnitine palmitoyltransferase and carnitine with autosomal dominant inheritance.

Authors: V Ionasescu; G Hug; C Hoppel
Journal: J Neurol Neurosurg Psychiatry Date: 1980-08 Impact factor: 10.154

Myoglobinuria in carnitine palmityltransferase deficiency.

1. A disorder of muscle lipid metabolism and myoglobinuria. Absence of carnitine palmityl transferase.

2. Myopathy due to a defect in muscle glycogen breakdown.

3. Recurrent myoglobinuria and muscle carnitine palmityltransferase deficiency.

4. Muscle phosphofructokinase deficiency.

5. Exercise myoglobinemia and acute exertional rhabdomyolysis.

6. Renal failure in McArdle's disease.

7. Combined partial deficiency of muscle carnitine palmitoyltransferase and carnitine with autosomal dominant inheritance.

8. Partial deficiency of carnitine palmityltransferase: physiologic and biochemical consequences.

9. Myoglobinuria, rhabdomyolysis and marathon running.

10. Disorders of lipid metabolism in muscle.

1. Rhabdomyolysis and myoglobinuria associated with violent exercise and alcohol abuse: report of two cases.