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Recurrent acute kidney injury and rhabdomyolysis: Questions

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References

  1. Vivante A, Ityel H, Pode-Shakked B, Chen J et al (2017) Exome sequencing in Jewish and Arab patients with rhabdomyolysis reveals single-gene etiology in 43% of cases. Pediatr Nephrol 32:2273–2282

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  2. Al-Ismaili Z, Piccioni M, Zappitelli M (2011) Rhabdomyolysis: pathogenesis of renal injury and management. Pediatr Nephrol 26:1781–1788

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  3. Mannix R, Tan ML, Wright R, Baskin M (2006) Acute pediatric rhabdomyolysis: causes and rates of renal failure. Pediatrics 118:2119–2125

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Authors and Affiliations

  1. Nephrology and Kidney Transplantation Unit, Department of Paediatrics, Santa Maria Hospital, Academic Center, Lisbon, Portugal

    Filipa Durão, Patrícia Valério & José E. Esteves da Silva

  2. Paediatric Service, Centro Hospitalar do Oeste, Lisbon, Portugal

    Bárbara Marques

  3. Genetics Service, Department of Paediatrics, Santa Maria Hospital, Academic Center, Lisbon, Portugal

    Raquel Gouveia Silva

  4. Metabolic Diseases Unit, Department of Paediatrics, Santa Maria Hospital, Academic Center, Lisbon, Portugal

    Patrícia Janeiro

Authors
  1. Filipa Durão
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  2. Patrícia Valério
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  3. Bárbara Marques
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  4. Raquel Gouveia Silva
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  5. Patrícia Janeiro
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  6. José E. Esteves da Silva
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Contributions

All authors contributed substantially to the design, interpretation and drafting of the case presented. All authors agree with the article contents and approve of the final version.

Corresponding author

Correspondence to Filipa Durão.

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Waived as it is a single case report.

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Written informed consent was obtained from the parents of the patient.

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The authors declare no competing interests.

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The answers to these questions can be found at https://doi.org/10.1007/s00467-021-05188-4

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Durão, F., Valério, P., Marques, B. et al. Recurrent acute kidney injury and rhabdomyolysis: Questions. Pediatr Nephrol 36, 4045–4046 (2021). https://doi.org/10.1007/s00467-021-05170-0

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  • DOI: https://doi.org/10.1007/s00467-021-05170-0

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