Light chain deposition disease without glomerular proteinuria: a diagnostic challenge for the nephrologist | Zendy

A Sicard | Zendy; Alexandre Karras | Zendy; Jean Michel Goujon | Zendy; Christophe Sirac | Zendy; Sébastien Bender | Zendy; D. Labatut | Zendy; P Callard | Zendy; Clémentine Sarkozy | Zendy; Marie Essig | Zendy; P. Vanhille | Zendy; François Provôt | Zendy; A. y | Zendy; Dominique Nochy | Zendy; P. Ronco | Zendy; Frank Bridoux | Zendy; Guy Touchard | Zendy

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Light chain deposition disease without glomerular proteinuria: a diagnostic challenge for the nephrologist

Author(s) -

A Sicard,

Alexandre Karras,

Jean Michel Goujon,

Christophe Sirac,

Sébastien Bender,

D. Labatut,

P Callard,

Clémentine Sarkozy,

Marie Essig,

P. Vanhille,

François Provôt,

A. y,

Dominique Nochy,

P. Ronco,

Frank Bridoux,

Guy Touchard

Publication year - 2014

Publication title -

nephrology dialysis transplantation

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 1.654

H-Index - 168

eISSN - 1460-2385

pISSN - 0931-0509

DOI - 10.1093/ndt/gfu045

Subject(s) - medicine , proteinuria , renal biopsy , monoclonal gammopathy of undetermined significance , renal function , pathology , kidney disease , gastroenterology , urology , focal segmental glomerulosclerosis , creatinine , nephrotic syndrome , glomerular basement membrane , kidney , monoclonal , immunology , antibody , monoclonal antibody

Renal involvement in light chain (LC) deposition disease (LCDD) is typically characterized by nodular glomerulosclerosis and nephrotic range proteinuria. Rare cases of LCDD without glomerular symptoms have been reported, but clinical and pathological characteristics of this entity remain poorly described.

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