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Comments on the letter of Galland et al. on “A rare cause of AA amyloidosis and end-stage kidney failure”

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References

  1. Durel CA, Aouba A, Bienvenu B et al (2016) Observational study of a French and Belgian multicenter cohort of 23 patients diagnosed in adulthood with mevalonate kinase deficiency. Medicine (United States). https://doi.org/10.1097/MD.0000000000003027

  2. Van Der Hilst JCH, Bodar EJ, Barron KS et al (2008) Long-term follow-up, clinical features, and quality of life in a series of 103 patients with hyperimmunoglobulinemia D syndrome. Medicine (Baltimore). https://doi.org/10.1097/MD.0b013e318190cfb7

  3. Obici L, Manno C, Muda AO et al (2004) First report of systemic reactive (AA) amyloidosis in a patient with the hyperimmunoglobulinemia D with periodic fever syndrome. Arthritis Rheum. https://doi.org/10.1002/art.20490

  4. Schlabe S, Schwarze-Zander C, Lohse P, Rockstroh JK (2016) Hyper-IgD and periodic fever syndrome (HIDS) due to compound heterozygosity for G336S and V377I in a 44-year-old patient with a 27-year history of fever. BMJ Case Rep. https://doi.org/10.1136/bcr-2016-217616

  5. Miray Kisla Ekinci R, Balcı S, Bisgin A et al (2019) Hyperimmunoglobulinemia D syndrome with recurrent perianal abscess successfully treated with canakinumab. Scott Med J. https://doi.org/10.1177/0036933019836405

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Authors and Affiliations

  1. Division of Pediatric Nephrology, Department of Pediatrics, Koç University School of Medicine, Istanbul, Turkey

    Mehmet Taşdemir, Sezen Yılmaz, Zeliha Füsun Baba & Ilmay Bilge

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  1. Mehmet Taşdemir
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  2. Sezen Yılmaz
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  3. Zeliha Füsun Baba
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  4. Ilmay Bilge
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Correspondence to Mehmet Taşdemir.

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Taşdemir, M., Yılmaz, S., Baba, Z.F. et al. Comments on the letter of Galland et al. on “A rare cause of AA amyloidosis and end-stage kidney failure”. Pediatr Nephrol 34, 1633–1634 (2019). https://doi.org/10.1007/s00467-019-04277-9

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  • DOI: https://doi.org/10.1007/s00467-019-04277-9

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