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  3. Myoglobinuria in two patients with Duchenne muscular dystrophy after treatment with zoledronate: a case-report and call for caution.
 

Myoglobinuria in two patients with Duchenne muscular dystrophy after treatment with zoledronate: a case-report and call for caution.

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BORIS DOI
10.7892/boris.120038
Publisher DOI
10.1016/j.nmd.2018.08.004
PubMed ID
30217487
Description
Rhabdomyolysis with myoglobinuria is a recognized complication of dystrophinopathies. It can be triggered by infections, exercise or volatile anesthetics. To our knowledge, it has never been reported in boys with Duchenne muscular dystrophy (DMD) after the administration of bisphosphonates. We report two patients with DMD who presented an apparent transient rhabdomyolysis with myoglobinuria after zoledronate administration. Possible mechanisms could involve hypophosphatemia, a known dose-dependent side effect of bisphosphonates, and/or direct myotoxicity of biphosphonates. Physicians and families should be aware of rhabdomyolysis with myoglobinuria as a potential uncommon side effect of bisphosphonates in DMD, in particular of zoledronate.
Date of Publication
2018-10
Publication Type
Article
Subject(s)
600 Technology > 610 Medicine & health
300 Social sciences, sociology & anthropology > 360 Social problems & social services
Keyword(s)
Duchenne muscular dystrophy bisphosphonates myoglobinuria zoledronate
Language(s)
en
Contributor(s)
Ivanyuk, Anton
García Segarra, Nuria
Buclin, Thierry
Klein, Andrea Katharina
Universitätsklinik für Kinderheilkunde, Neuropädiatrie
Jacquier, David
Newman, Christopher J
Blötzer, Clemens Florian
Institut für Sozial- und Präventivmedizin (ISPM)
Additional Credits
Universitätsklinik für Kinderheilkunde, Neuropädiatrie
Institut für Sozial- und Präventivmedizin (ISPM)
Series
Neuromuscular disorders
Publisher
Elsevier
ISSN
0960-8966
Access(Rights)
open.access
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