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Myoglobinuria in boys with Duchenne muscular dystrophy on corticosteroid therapy

Lookup NU author(s): Dr Penelope Garrood, Dr Michelle Eagle, Emerita Professor Katherine Bushby, Professor Volker Straub

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Abstract

Myoglobinuria is a recognised complication of Duchenne muscular dystrophy (DMD), but has only once been reported in ambulant boys on corticosteroid therapy [Dubowitz V, Kinali M, Main M, Mercuri E, Muntoni F. Remission of clinical signs in early Duchenne muscular dystrophy on intermittent low-dosage prednisolone therapy. Eur J Paediatr Neurol 2002;6(3):153-9.]. We present three prednisolone-treated boys with myoglobinuria and in two cases this was recurrent. All three showed improved motor performance in response to the introduction of corticosteroids. The greater activity of steroid-treated individuals may place their dystrophin-deficient muscles under greater mechanical stress, predisposing to further muscle fibre damage and consequent myoglobinuria. Families and physicians need to have an increased awareness of this possibility and of the appropriate management of myoglobinuria. © 2007 Elsevier B.V. All rights reserved.


Publication metadata

Author(s): Garrood PVA, Eagle M, Jardine PE, Bushby KMD, Straub VW

Publication type: Article

Publication status: Published

Journal: Neuromuscular Disorders

Year: 2008

Volume: 18

Issue: 1

Pages: 71-73

Print publication date: 01/01/2008

ISSN (print): 0960-8966

ISSN (electronic): 1873-2364

Publisher: Elsevier

URL: http://dx.doi.org/10.1016/j.nmd.2007.07.006

DOI: 10.1016/j.nmd.2007.07.006

PubMed id: 17719224


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