|OtoSCOPE provides comprehensive genetic testing for all genes implicated in non-syndromic hearing loss and many types of syndromic hearing loss. An Usher Syndrome Panel is also available.||Genetic Renal Panel screens patients diagnosed with thrombotic microangiopathies and C3 glomerulopathy. The next-generation sequencing panel includes analysis of 12 genes for single nucleotide variants as well as MLPA, which identifies copy-number variations in the CFH-CFHR5 genomic region.||Comprehensive complement testing includes quantitating complement proteins and their cleavage products, measuring complement activity, and screening for autoantibodies.|
- Your results are discussed at a multidisciplinary meeting.
- Your testing is performed in the Clinical Division of the MORL by scientists who lead the world in the human genetics of deafness and complement-mediated renal diseases.
- Our testing is the most comprehensive clinical testing available.
C3G Educational Day for Nephrologists: April 18, 2020: Postponed due to COVID19
16th DDD/C3G Family Conference: