Myoglobinuria

Evidence-based neurology checklist on myoglobinuria: Neurological causes Rhabdomyolysis Myopathies Polymyositis McArdle’s disease Phosphofructokinase deficiency (Tarui disease) Central core disease Dystrophinopathy Limb girdle muscular dystrophy type 2D (LGMD 2A) Seizures Hereditary myopathy with…

Neurological causes

  • Rhabdomyolysis
  • Myopathies
  • Polymyositis
  • McArdle’s disease
  • Phosphofructokinase deficiency (Tarui disease)
  • Central core disease
  • Dystrophinopathy
  • Limb girdle muscular dystrophy type 2D (LGMD 2A)
  • Seizures
  • Hereditary myopathy with lactic acidosis, succinate dehydrogenase and aconitase deficiency

Non-neurological causes

References

  1. Ellis CJ, Dewhurst AG, Cooper M, Brenton DP, Dathan JRE. Myoglobinuria: the importance of reaching a firm diagnosis-a patient with defective fatty acid oxidation. Postgrad Med J 1990; 66:235-237.
  2. De Bleeker JL. How to approach the patient with muscular symptoms in the general neurological practice? Acta Neurol Belg 2005; 105:18-22.
  3. Chawla J. Stepwise approach to myopathy in systemic disease. Front Neurol 2011; 2:49.
  4. Doriguzzi C, Palmucci L, Mongini T, et al. Exercise intolerance and recurrent myoglobinuria as there only expression of Xp21 Becker type muscular dystrophy. J Neurol 1993; 240:269-271.
  5. Sanchez-Arjona MB, Rodriguez-Uranga JJ, Giles-Lima M, et al. Spanish family with myalgia and cramps syndrome. JNNP 2005; 76:286-289.
  6. And 5 more. Subscribe to see the full list

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