loading...| Preferred Name | Light chain deposition disease | |
| Synonyms |
LCDD |
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| Definitions |
A rare non-amyloid monoclonal immunoglobulin deposition disease characterized by deposition of abnormal immunoglobulin light chains in the kidneys, resulting in nephrotic syndrome and renal failure. Symptomatic extrarenal deposition is uncommon, although hepatic, cardiac, and neural deposits have been reported. The condition frequently occurs in association with multiple myeloma or in patients with M protein and marrow plasma cells at monoclonal gammopathy of undetermined significance levels. |
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| ID |
http://www.orpha.net/ORDO/Orphanet_93558 |
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| alternative_term |
LCDD |
|
| definition |
A rare non-amyloid monoclonal immunoglobulin deposition disease characterized by deposition of abnormal immunoglobulin light chains in the kidneys, resulting in nephrotic syndrome and renal failure. Symptomatic extrarenal deposition is uncommon, although hepatic, cardiac, and neural deposits have been reported. The condition frequently occurs in association with multiple myeloma or in patients with M protein and marrow plasma cells at monoclonal gammopathy of undetermined significance levels. |
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| definition_citation |
Orphanet |
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| expertlink |
https://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=en&Expert=93558 |
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| hasDbXref |
ICD-11:2A83.52 UMLS:C0238239 ICD-10:D89.8 |
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| label |
Light chain deposition disease |
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| notation |
ORPHA:93558 Clinical subtype |
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| part_of | ||
| prefixIRI |
ORDO:Orphanet_93558 |
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| prefLabel |
Light chain deposition disease |
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| treeView | ||
| subClassOf |