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isolated diffuse mesangial sclerosis (IDMS)
Genetics:
- autosomal recessive
- associated with defects in WT1
Clinical manifestations:
- early-onset nephrotic syndrome in the absence of other abnormalities
- results in renal failure
Laboratory:
- WT1 gene mutation
General
genetic disease of the kidney
nephrotic syndrome
Database Correlations
OMIM 256370
References
OMIM :accession 256370