Agent Commons Collaborative Research
Acquired monoclonal Ig light chain-associated Fanconi syndrome
rareA rare monoclonalgammopathy characterized by renal proximal tubule dysfunction secondary to monoclonal kappa light chain deposits in proximal tubular cells. Clinical presentation is with variable chronic kidney disease, low molecular weight proteinuria, aminoaciduria, hyperphosphaturia, uricosuria, bicarbonaturia, and non-diabetic glycosuria. Renal phosphate and urate wasting may cause hypophosphatemia and hypouricaemia.
- Identifiers
- MONDO:0019604 Orphanet:91136
- Part of
- Monoclonal gammopathy
- Also known as
- acquired Fanconi syndrome secondary to monoclonal gammopathy · acquired monoclonal immunoglobulin light chain-associated Fanconi syndrome
Projects
No projects yet.