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Pediatric Nephrology

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01-09-2019 | Chronic Inflammatory Bowel Disease | Letter to the Editors

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

Authors: Mehmet Taşdemir, Sezen Yılmaz, Zeliha Füsun Baba, Ilmay Bilge

Published in: Pediatric Nephrology | Issue 9/2019

Excerpt

Dear Editor, …

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

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

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

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

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

Title: Comments on the letter of Galland et al. on “A rare cause of AA amyloidosis and end-stage kidney failure”
Authors: Mehmet Taşdemir
Sezen Yılmaz
Zeliha Füsun Baba
Ilmay Bilge
Publication date: 01-09-2019
Publisher: Springer Berlin Heidelberg
Keywords: Chronic Inflammatory Bowel Disease
Nephrotic Syndrome
AA Amyloidosis
Autoinflammatory Diseases
Familial Mediterranean Fever
Published in: Pediatric Nephrology / Issue 9/2019
Print ISSN: 0931-041X
Electronic ISSN: 1432-198X
DOI: https://doi.org/10.1007/s00467-019-04277-9

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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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