A unique case of light chain (AL) amyloidosis masquerading as hypophosphatemic osteomalacia
Author:
Publisher
Springer Science and Business Media LLC
Subject
Endocrinology, Diabetes and Metabolism
Link
https://link.springer.com/content/pdf/10.1007/s00198-020-05622-7.pdf
Reference18 articles.
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2. Leung N, Bridoux F, Batuman V et al (2019) The evaluation of monoclonal gammopathy of renal significance: a consensus report of the International Kidney and Monoclonal Gammopathy Research Group. Nat Rev Nephrol 15(1):45–59
3. Kyle RA, Gertz MA (1995) Primary systemic amyloidosis: clinical and laboratory features in 474 cases. Semin Hematol 32:45–59
4. Palladini G, Russo P, Bosoni T et al (2009) Identification of amyloidogenic light chains requires the combination of serum-free light chain assay with immunofixation of serum and urine. Clin Chem 55(3):499
5. Novak L, Cook WJ, Herrera GA, Sanders PW (2004) AL-amyloidosis is underdiagnosed in renal biopsies. Nephrol Dial Transplant 19(12):3050–3053
Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Adult-onset hypophosphatemic osteomalacia as a cause of widespread musculoskeletal pain: A retrospective case series of single center experience;World Journal of Clinical Cases;2023-11-16
2. Consensus Recommendations for the Diagnosis and Management of X-Linked Hypophosphatemia in Belgium;Frontiers in Endocrinology;2021-03-19
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