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A case of hypoparathyroidism, sensorineural deafness, and renal dysplasia syndrome with kidney failure and recurrent pancreatitis: Questions

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We thank Editage (www.editage.jp) for the English language editing.

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Toshihiro Abe, Yuji Hidaka, Shinya Kawamoto, Tadahiko Tokumoto, and Atsunori Yoshino were the attending physicians during hospital treatment and at the outpatient clinic. Atsunori Yoshino wrote the manuscript. Koji Muroya performed genetic examinations and determined the genetic diagnosis. Tadahiko Tokumoto performed pre-emptive kidney transplantation. Atsunori Yoshino and Tadahiko Tokumoto provided medical care during hospitalization and at the outpatient treatment after kidney transplantation. Tetsuro Takeda provided medical care during hospitalization and revised the manuscript. All authors have read the final version of this paper and approved its publication.

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Correspondence to Atsunori Yoshino.

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This report has been approved by the research ethics committee of Dokkyo Medical University Saitama Medical Center (ID: 21035).

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Written informed consent was obtained from the patient and his parents for publication of this case report, including clinical information. The consent form has been stored by the corresponding author and may be obtained upon request from the editor of this journal.

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The answers to these questions can be found at https://doi.org/10.1007/s00467-021-05190-w

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Yoshino, A., Kawamoto, S., Abe, T. et al. A case of hypoparathyroidism, sensorineural deafness, and renal dysplasia syndrome with kidney failure and recurrent pancreatitis: Questions. Pediatr Nephrol 36, 4067–4069 (2021). https://doi.org/10.1007/s00467-021-05183-9

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